Canonical Allele Identifier: PA2828881167
Gene: UCP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 130697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001368876.1:p.Ala55Val
CA155899
NM_001381947.1:c.164C>T