Canonical Allele Identifier: PA2827936701
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691832
ClinVar RCV Id: RCV003494029
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val226Leu
CA367401125
NM_001354800.1:c.676G>C
CA367401128
NM_001354800.1:c.676G>T