Canonical Allele Identifier: PA2827937118
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2628365
ClinVar RCV Id: RCV003397220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ala41Pro
CA367398808
NM_001354801.1:c.121G>C