Canonical Allele Identifier: PA100838
Gene: CPOX HGNC NCBI
ClinVar RCV:
RCV000000492
ClinVar Variation:
463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000088.3:p.Gly279Arg
CA114304
NM_000097.7:c.835G>C