Canonical Allele Identifier: PA2829298687
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004310436
ClinVar Variation:
2534102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387222.1:p.Lys1186Arg
CA2392566
NM_001400293.1:c.3557A>G