Canonical Allele Identifier: PA2829181680
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004212269
ClinVar Variation:
2371430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376531.1:p.Thr552Asn
CA2393068
NM_001389602.1:c.1655C>A