Allele Registry

Canonical Allele Identifier: PA2828881052

Gene: UCP2 HGNC NCBI

ClinVar RCV:

RCV000118811

RCV001682828

ClinVar Variation:

130697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001368873.1:p.Ala55Val	CA155899 NM_001381944.1:c.164C>T