Canonical Allele Identifier: PA100905
Gene: CPOX HGNC NCBI
ClinVar RCV:
RCV000000489
ClinVar Variation:
460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000088.3:p.Ser208Phe
CA114302
NM_000097.7:c.623C>T