Canonical Allele Identifier: PA916039371
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393447
ClinVar RCV Id: RCV000445420 RCV001584122 RCV004539920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ala74Glu
CA16609264
NM_001354802.1:c.221C>A