Canonical Allele Identifier: PA2579978002
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu270Pro
CA367400510
NM_000162.5:c.809T>C