Canonical Allele Identifier: PA645420866
Gene: CPOX HGNC NCBI

Linked Data

ClinVar Variation Id: 346987
ClinVar RCV Id: RCV000373961 RCV001753816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000088.3:p.Glu100Val
CA2511736
NM_000097.7:c.299A>T