Canonical Allele Identifier: PA2827936406
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 420070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gln38Pro
CA16618475
NM_001354800.1:c.113A>C