Canonical Allele Identifier: PA100856
Gene: CPOX HGNC NCBI
ClinVar RCV:
RCV000000485
ClinVar Variation:
456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000088.3:p.His295Asp
CA114298
NM_000097.7:c.883C>G