Canonical Allele Identifier: PA2580490773
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700679
ClinVar RCV Id: RCV002285557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val155Ala
CA367401909
NM_033507.3:c.464T>C