Canonical Allele Identifier: PA121279
Gene: GK HGNC NCBI

Linked Data

ClinVar Variation Id: 10948
ClinVar RCV Id: RCV000011695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_976325.1:p.Asn294Asp
CA121276
NM_203391.4:c.880A>G