Canonical Allele Identifier: PA2829299053
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004293295
ClinVar Variation:
2512894
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387227.1:p.Arg640Gln
CA352749112
NM_001400298.1:c.1919G>A