Canonical Allele Identifier: PA2829299160
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004310436
ClinVar Variation:
2534102
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387228.1:p.Lys1163Arg
CA2392566
NM_001400299.1:c.3488A>G