Canonical Allele Identifier: PA2830123272
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2502089
ClinVar RCV Id: RCV003228508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala187Pro
CA367401562
NM_033508.3:c.559G>C