Canonical Allele Identifier: PA2579974966
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700679
ClinVar RCV Id: RCV002285557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val154Ala
CA367401909
NM_000162.5:c.461T>C