Canonical Allele Identifier: PA645460338
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36268
ClinVar RCV Id: RCV000029931 RCV002472939 RCV002371789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly319Trp
CA213870
NM_033507.3:c.955G>T