Canonical Allele Identifier: PA2830123782
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2632567
ClinVar RCV Id: RCV003416862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg368Pro
CA367398967
NM_033508.3:c.1103G>C