Product Details

SNP ID

hCV30024733

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:165258455 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGGTTATTTTTAATCAATCTCAG[T/G]GTTAACACTAGTGCAACTCTGCACT

Phenotype

MIM: 605774

Polymorphism

T/G, Transversion substitution

Allele Nomenclature

Literature Links

KLHL2 PubMed Links

Gene Details

Gene

KLHL2

Gene Name

kelch like family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001161521.1		Intron			NP_001154993.1
NM_001161522.1		Intron			NP_001154994.1
NM_007246.3		Intron			NP_009177.3

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