Canonical Allele Identifier: PA2829298922
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004263351
ClinVar Variation:
2468045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387225.1:p.Arg1302Trp
CA2392475
NM_001400296.1:c.3904C>T