Canonical Allele Identifier: PA2829649016
Gene: USP19 HGNC NCBI
ClinVar RCV:
RCV004263807
ClinVar Variation:
2470351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006668.1:p.Val1304Met
CA2392409
NM_006677.3:c.3910G>A