Allele Registry

Canonical Allele Identifier: PA2830123362

Gene: GCK HGNC NCBI

ClinVar Allele:

44897

ClinVar RCV:

RCV000029896

RCV000711779

RCV003445084

ClinVar Variation:

36233

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Met201Thr	CA213810 NM_033508.3:c.602T>C