Canonical Allele Identifier: PA2741997570
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735011
ClinVar RCV Id: RCV003555338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Cys214Arg
CA367401273
NM_033507.3:c.640T>C