Allele Registry

Canonical Allele Identifier: PA2573296649

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV002227423

ClinVar Variation:

1679544

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Asp206Val	CA367401343 NM_033507.3:c.617A>T