Canonical Allele Identifier: PA2827936808
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136513
ClinVar RCV Id: RCV003037215
ClinVar Variation Id: 2735003
ClinVar RCV Id: RCV003555334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp278Glu
CA367400460
NM_001354800.1:c.834C>G
CA367400461
NM_001354800.1:c.834C>A