Canonical Allele Identifier: PA2830123301
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2499721
ClinVar RCV Id: RCV003223813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg191Ser
CA367401516
NM_033508.3:c.573A>T
CA367401517
NM_033508.3:c.573A>C