Canonical Allele Identifier: PA2579982620
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1770532
ClinVar RCV Id: RCV002387880 RCV003774278
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala450Ser
CA367396909
NM_000162.5:c.1348G>T