Canonical Allele Identifier: PA2830123172
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1743101
ClinVar RCV Id: RCV002330710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asp159His
CA367401848
NM_033508.3:c.475G>C