Canonical Allele Identifier: PA213772
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36209
ClinVar RCV Id: RCV000029872 RCV000255585 RCV001248967 RCV002426523
ClinVar Variation Id: 976334
ClinVar RCV Id: RCV001253600 RCV003546683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly72Arg
CA213771
NM_000162.5:c.214G>A
CA367403112
NM_000162.5:c.214G>C