Canonical Allele Identifier: PA645460232
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435306
ClinVar RCV Id: RCV000502130 RCV000517681 RCV000763585 RCV002367690 RCV003403165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly224Ser
CA367401165
NM_033507.3:c.670G>A