Canonical Allele Identifier: PA2580102536
Gene: CPOX HGNC NCBI

Linked Data

ClinVar Variation Id: 1716081
ClinVar RCV Id: RCV002295849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000088.3:p.Arg359Ser
CA353644998
NM_000097.7:c.1077G>C
CA353644999
NM_000097.7:c.1077G>T