Canonical Allele Identifier: PA2827936740
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804856
ClinVar RCV Id: RCV000992062 RCV002382224 RCV003446565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly246Ala
CA367400661
NM_001354800.1:c.737G>C