Canonical Allele Identifier: PA2579975998
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2881307
ClinVar RCV Id: RCV003715883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr118Ser
CA367402572
NM_000162.5:c.353C>G
CA367402575
NM_000162.5:c.352A>T