Canonical Allele Identifier: PA174799
Gene: RPUSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161795
ClinVar RCV Id: RCV000149331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478072.1:p.His174Arg
CA174798
NM_058192.3:c.521A>G