Canonical Allele Identifier: PA350523
Gene: UVRAG HGNC NCBI

Linked Data

ClinVar Variation Id: 219329
ClinVar RCV Id: RCV000206501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003360.2:p.Glu167Gly
CA350522
NM_003369.4:c.500A>G