Canonical Allele Identifier: PA2829182030
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004293295
ClinVar Variation:
2512894
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376535.1:p.Arg557Gln
CA352749112
NM_001389606.1:c.1670G>A