Canonical Allele Identifier: PA2829180967
Gene: USP19 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376523.1:p.Arg180His
CA2393359
NM_001389594.1:c.539G>A