Canonical Allele Identifier: PA2579975094
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1309623
ClinVar RCV Id: RCV001765792
ClinVar Variation Id: 1685845
ClinVar RCV Id: RCV002250012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Trp167Cys
CA367401757
NM_000162.5:c.501G>T
CA367401759
NM_000162.5:c.501G>C