Canonical Allele Identifier: PA127418
Gene: ATP2A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001672.1:p.Asn767Ser
CA127417
NM_001681.4:c.2300A>G