Canonical Allele Identifier: PA2830123920
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2169517
ClinVar RCV Id: RCV003084866 RCV003318514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg393Pro
CA367398581
NM_033508.3:c.1178G>C
CA2695203000
NM_033508.3:c.1178_1179delinsCG