Canonical Allele Identifier: PA2580251628
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004263807
ClinVar Variation:
2470351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387217.1:p.Val1407Met
CA2392409
NM_001400288.1:c.4219G>A