Allele Registry

Canonical Allele Identifier: PA119887

Gene: GCKR HGNC NCBI

ClinVar RCV:

RCV000009294

RCV001618209

RCV002182980

ClinVar Variation:

8751

1549832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001477.2:p.Leu446Pro	CA119886 NM_001486.4:c.1337T>C CA2573134442 NM_001486.4:c.1337_1338delinsCC