Allele Registry

Canonical Allele Identifier: PA155900

Gene: UCP2 HGNC NCBI

ClinVar RCV:

RCV000118811

RCV001682828

ClinVar Variation:

130697

HGVS (amino-acid)	Matching Registered Transcripts
NP_003346.2:p.Ala55Val	CA155899 NM_003355.2:c.164C>T