Allele Registry

Canonical Allele Identifier: PA213697

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029827

RCV002463591

ClinVar Variation:

36164

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Phe334_Val335delinsLeuMet	CA213696 NM_000162.5:c.1002_1003delinsAA