Canonical Allele Identifier: PA2829298779
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004334952
ClinVar Variation:
2591163
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387224.1:p.Arg221Gln
CA2393313
NM_001400295.1:c.662G>A