Canonical Allele Identifier: PA110192
Gene: ATP1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12919
ClinVar RCV Id: RCV000013782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000693.1:p.Met731Thr
CA256631
NM_000702.4:c.2192T>C