Canonical Allele Identifier: PA1139735196
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 987827
ClinVar RCV Id: RCV001269172 RCV001880174 RCV002463800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Arg8Gly
CA367399354
NM_001354801.1:c.22C>G