Canonical Allele Identifier: PA2579975657
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2775417
ClinVar RCV Id: RCV003577094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser360Leu
CA367399114
NM_000162.5:c.1079C>T