Canonical Allele Identifier: PA2827936748
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1678597
ClinVar RCV Id: RCV002225198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met251Val
CA367400634
NM_001354800.1:c.751A>G