Allele Registry

Canonical Allele Identifier: PA645460204

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029897

RCV002463603

RCV002475240

RCV002513252

ClinVar Variation:

36234

1807283

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Asp206Glu	CA213812 NM_033507.3:c.618C>G CA367401342 NM_033507.3:c.618C>A