Canonical Allele Identifier: PA2829298691
Gene: USP19 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387222.1:p.Arg1315Trp
CA2392475
NM_001400293.1:c.3943C>T