Canonical Allele Identifier: PA2825042356
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1743101
ClinVar RCV Id: RCV002330710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp160His
CA367401848
NM_000162.5:c.478G>C