Canonical Allele Identifier: PA2827587650
Gene: USP19 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338031.1:p.Lys1072Arg
CA2392566
NM_001351102.2:c.3215A>G