Canonical Allele Identifier: PA2829182138
Gene: USP19 HGNC NCBI

Linked Data

ClinVar Variation Id: 2457594
ClinVar RCV Id: RCV004248729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001376536.1:p.Met969Leu
CA2392644
NM_001389607.1:c.2905A>T
CA352735964
NM_001389607.1:c.2905A>C