Canonical Allele Identifier: PA303508
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189996
ClinVar RCV Id: RCV000180952 RCV001850422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala420Val
CA303506
NM_001165963.4:c.1259C>T