Canonical Allele Identifier: PA2827240392
Gene: RPUSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161795
ClinVar RCV Id: RCV000149331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311015.1:p.His177Arg
CA174798
NM_001324086.2:c.530A>G