Canonical Allele Identifier: PA212741
Gene: CPOX HGNC NCBI
ClinVar RCV:
RCV000000484
ClinVar Variation:
455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000088.3:p.Cys164_Val170del
CA212740
NM_000097.7:c.489_509del