Canonical Allele Identifier: PA2830122799
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972774
ClinVar RCV Id: RCV001248984 RCV003481036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly67Asp
CA157919943
NM_033508.3:c.200G>A