Canonical Allele Identifier: PA102919
Gene: ATP2A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17792
ClinVar RCV Id: RCV000493249 RCV002288512 RCV000019370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733765.1:p.Asn767Ser
CA127417
NM_170665.4:c.2300A>G