Canonical Allele Identifier: PA2827936667
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447411
ClinVar RCV Id: RCV000517275 RCV002367713 RCV003493616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala208Val
CA4239569
NM_001354800.1:c.623C>T