Canonical Allele Identifier: PA096170
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 431973
ClinVar RCV Id: RCV000497478 RCV000503648 RCV000788107 RCV003403150
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg36Trp
CA4239720
NM_000162.5:c.106C>T