Canonical Allele Identifier: PA2829298629
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004334952
ClinVar Variation:
2591163
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387222.1:p.Arg237Gln
CA2393313
NM_001400293.1:c.710G>A