Canonical Allele Identifier: PA645420852
Gene: CPOX HGNC NCBI

Linked Data

ClinVar Variation Id: 346993
ClinVar RCV Id: RCV000397238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000088.3:p.Ala44Ser
CA10619762
NM_000097.7:c.130G>T