Allele Registry

Canonical Allele Identifier: PA916039398

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029842

RCV002463594

RCV002958450

ClinVar Variation:

36179

2065408

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341732.1:p.Gly63Arg	CA213721 NM_001354803.2:c.187G>A CA367398717 NM_001354803.2:c.187G>C