Allele Registry

Canonical Allele Identifier: PA3057340119

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV004702128

ClinVar Variation:

3338871

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Asp197Val	CA367401416 NM_033508.3:c.590A>T