Allele Registry

Canonical Allele Identifier: PA100787

Gene: CPOX HGNC NCBI

ClinVar RCV:

RCV000000480

RCV003989277

ClinVar Variation:

451

HGVS (amino-acid)	Matching Registered Transcripts
NP_000088.3:p.Arg331Trp	CA114296 NM_000097.7:c.991C>T