Canonical Allele Identifier: PA2830123991
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2571660
ClinVar RCV Id: RCV003313370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe418Val
CA367397313
NM_033508.3:c.1252T>G