Canonical Allele Identifier: PA2827937223
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ser104Leu
CA367397015
NM_001354801.1:c.311C>T