Canonical Allele Identifier: PA2829181102
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004293295
ClinVar Variation:
2512894
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376524.1:p.Arg658Gln
CA352749112
NM_001389595.1:c.1973G>A