Canonical Allele Identifier: PA2827587698
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2371430
ClinVar RCV Id: RCV004212269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338032.1:p.Thr454Asn
CA2393068
NM_001351103.2:c.1361C>A