Canonical Allele Identifier: PA2829181247
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004213563
ClinVar Variation:
2377248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376526.1:p.Ile738Thr
CA2392832
NM_001389597.1:c.2213T>C