Allele Registry

Canonical Allele Identifier: PA2579982595

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003993704

ClinVar Variation:

3068512

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Ala454Val	CA367396861 NM_000162.5:c.1361C>T