Canonical Allele Identifier: PA2830123507
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691830
ClinVar RCV Id: RCV003494027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg249Pro
CA367400637
NM_033508.3:c.746G>C