Canonical Allele Identifier: PA645460195
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36231
ClinVar RCV Id: RCV000029894 RCV002463601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Glu197Gly
CA213806
NM_033507.3:c.590A>G