Canonical Allele Identifier: PA2579974962
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2682650
ClinVar RCV Id: RCV003481517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val154Gly
CA367401907
NM_000162.5:c.461T>G