Canonical Allele Identifier: PA303597
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190028
ClinVar RCV Id: RCV000180984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Tyr1274Ser
CA303594
NM_001165963.4:c.3821A>C