Canonical Allele Identifier: PA2830123557
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1479681
ClinVar RCV Id: RCV002009866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala258Asp
CA367400580
NM_033508.3:c.773C>A