Canonical Allele Identifier: PA103032
Gene: ATP2A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733765.1:p.Gly769Arg
CA127425
NM_170665.4:c.2305G>A
CA386675855
NM_170665.4:c.2305G>C