Allele Registry

Canonical Allele Identifier: PA151149

Gene: CPOX HGNC NCBI

ClinVar RCV:

RCV000114373

ClinVar Variation:

126445

HGVS (amino-acid)	Matching Registered Transcripts
NP_000088.3:p.His327Arg	CA151148 NM_000097.7:c.980A>G