Canonical Allele Identifier: PA2830122037
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2632567
ClinVar RCV Id: RCV003416862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg370Pro
CA367398967
NM_033507.3:c.1109G>C