Canonical Allele Identifier: PA2579975143
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2580858
ClinVar RCV Id: RCV003330053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val226Gly
CA367401120
NM_000162.5:c.677T>G