Canonical Allele Identifier: PA096193
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735011
ClinVar RCV Id: RCV003555338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys213Arg
CA367401273
NM_000162.5:c.637T>C