Canonical Allele Identifier: PA2829181724
Gene: USP19 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376531.1:p.Val1404Met
CA2392409
NM_001389602.1:c.4210G>A