Canonical Allele Identifier: PA2827587544
Gene: USP19 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338030.1:p.Arg658Gln
CA352749112
NM_001351101.2:c.1973G>A