Canonical Allele Identifier: PA2741868016
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691824
ClinVar RCV Id: RCV003494021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ile99Phe
CA367397094
NM_001354801.1:c.295A>T