Canonical Allele Identifier: PA303142
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189863
ClinVar RCV Id: RCV000180816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Leu863Trp
CA303139
NM_001165963.4:c.2588T>G