Canonical Allele Identifier: PA2579980720
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 810090
ClinVar RCV Id: RCV000998793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys252Phe
CA367400622
NM_000162.5:c.755G>T