Canonical Allele Identifier: PA100778
Gene: CPOX HGNC NCBI

Linked Data

ClinVar Variation Id: 461
ClinVar RCV Id: RCV000000490

Amino-acid Alleles

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