Canonical Allele Identifier: PA2829182058
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2534102
ClinVar RCV Id: RCV004310436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376535.1:p.Lys1087Arg
CA2392566
NM_001389606.1:c.3260A>G