Canonical Allele Identifier: PA2829181716
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004263351
ClinVar Variation:
2468045
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376531.1:p.Arg1314Trp
CA2392475
NM_001389602.1:c.3940C>T