Allele Registry

Canonical Allele Identifier: PA645461042

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029842

RCV002463594

RCV002958450

ClinVar Variation:

36179

2065408

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Gly386Arg	CA213721 NM_033507.3:c.1156G>A CA367398717 NM_033507.3:c.1156G>C