Canonical Allele Identifier: PA2829298462
Gene: USP19 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387219.1:p.Arg180His
CA2393359
NM_001400290.1:c.539G>A