Allele Registry

Canonical Allele Identifier: PA2830122767

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000431394

RCV000479407

RCV002402377

ClinVar Variation:

377026

418225

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Met56Ile	CA16603236 NM_033508.3:c.168G>T CA16618473 NM_033508.3:c.168G>A CA367403315 NM_033508.3:c.168G>C