Canonical Allele Identifier: PA2829299060
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004149418
ClinVar Variation:
2307265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387227.1:p.Ile782Phe
CA2392893
NM_001400298.1:c.2344A>T