Canonical Allele Identifier: PA2830122696
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393453
ClinVar RCV Id: RCV000445457 RCV000711763 RCV002285330 RCV002379402 RCV003418141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg42His
CA4239718
NM_033508.3:c.125G>A