Canonical Allele Identifier: PA100778
Gene: CPOX HGNC NCBI
ClinVar RCV:
RCV000000490
ClinVar Variation:
461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000088.3:p.Arg328Cys
CA114303
NM_000097.7:c.982C>T