Allele Registry

Canonical Allele Identifier: PA213811

Gene: GCK HGNC NCBI

MaveDb:

Score 0.050090141

ClinVar Allele:

44897

ClinVar RCV:

RCV000029896

RCV000711779

RCV003445084

ClinVar Variation:

36233

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Met202Thr	CA213810 NM_000162.5:c.605T>C