Allele Registry

Canonical Allele Identifier: PA2579976910

Gene: GCK HGNC NCBI

MaveDb:

Score -0.081699748

ClinVar RCV:

RCV000431394

RCV000479407

RCV002402377

ClinVar Variation:

377026

418225

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Met57Ile	CA16603236 NM_000162.5:c.171G>T CA16618473 NM_000162.5:c.171G>A CA367403315 NM_000162.5:c.171G>C