Canonical Allele Identifier: PA645460198
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36232
ClinVar RCV Id: RCV000029895 RCV002463602 RCV003883123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met203Val
CA213808
NM_033507.3:c.607A>G