Canonical Allele Identifier: PA2827771289
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1321314
ClinVar RCV Id: RCV001779411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Tyr1411Phe
CA349049898
NM_001353951.2:c.4232A>T