Canonical Allele Identifier: PA2829181778
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004293295
ClinVar Variation:
2512894
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376532.1:p.Arg643Gln
CA352749112
NM_001389603.1:c.1928G>A