Allele Registry

Canonical Allele Identifier: PA2827936651

Gene: GCK HGNC NCBI

ClinVar Allele:

44897

ClinVar RCV:

RCV000029896

RCV000711779

RCV003445084

ClinVar Variation:

36233

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Met202Thr	CA213810 NM_001354800.1:c.605T>C