Canonical Allele Identifier: PA2827587701
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004293295
ClinVar Variation:
2512894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338032.1:p.Arg557Gln
CA352749112
NM_001351103.2:c.1670G>A