Canonical Allele Identifier: PA2829676714
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1715838
ClinVar RCV Id: RCV002304639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Phe1929Tyr
CA349063678
NM_006920.6:c.5786T>A