Canonical Allele Identifier: PA2829182039
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004213563
ClinVar Variation:
2377248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376535.1:p.Ile736Thr
CA2392832
NM_001389606.1:c.2207T>C