Canonical Allele Identifier: PA100842
Gene: ATP1A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 12913
ClinVar RCV Id: RCV000013776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689509.1:p.Phe780Leu
CA341237
NM_152296.5:c.2338T>C
CA406039520
NM_152296.5:c.2340C>G
CA406039522
NM_152296.5:c.2340C>A