Canonical Allele Identifier: PA2829181500
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2371430
ClinVar RCV Id: RCV004212269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376529.1:p.Thr538Asn
CA2393068
NM_001389600.1:c.1613C>A