Canonical Allele Identifier: PA303392
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189952
ClinVar RCV Id: RCV000180905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala1339Val
CA303389
NM_001165963.4:c.4016C>T