Canonical Allele Identifier: PA256649
Gene: ATP1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000693.1:p.Ile286Thr
CA256647
NM_000702.4:c.857T>C