Canonical Allele Identifier: PA2829181142
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2470351
ClinVar RCV Id: RCV004263807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376524.1:p.Val1407Met
CA2392409
NM_001389595.1:c.4219G>A