Canonical Allele Identifier: PA102967
Gene: ATP2A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17794
ClinVar RCV Id: RCV000019372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733765.1:p.Cys560Arg
CA127421
NM_170665.4:c.1678T>C