Allele Registry

Canonical Allele Identifier: PA2829121781

Gene: UVRAG HGNC NCBI

ClinVar RCV:

RCV004078698

ClinVar Variation:

2217744

HGVS (amino-acid)	Matching Registered Transcripts
NP_001373600.1:p.Thr212Ile	CA381978067 NM_001386671.1:c.635C>T