Canonical Allele Identifier: PA916039396
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 236014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ser61Leu
CA10581499
NM_001354803.2:c.182C>T