Canonical Allele Identifier: PA2829299164
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004263351
ClinVar Variation:
2468045
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387228.1:p.Arg1292Trp
CA2392475
NM_001400299.1:c.3874C>T