Canonical Allele Identifier: PA121278
Gene: GK HGNC NCBI

Linked Data

ClinVar Variation Id: 10948
ClinVar RCV Id: RCV000011695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121599.1:p.Asn288Asp
CA121276
NM_001128127.3:c.862A>G