Canonical Allele Identifier: PA2827587485
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004263351
ClinVar Variation:
2468045
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338029.1:p.Arg1316Trp
CA2392475
NM_001351100.2:c.3946C>T