Canonical Allele Identifier: PA2579976088
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435298
ClinVar RCV Id: RCV000499850 RCV003313087 RCV003482262
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser441Leu
CA367397015
NM_000162.5:c.1322C>T