Canonical Allele Identifier: PA2827587891
Gene: USP19 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338034.1:p.Lys1136Arg
CA2392566
NM_001351105.2:c.3407A>G