Canonical Allele Identifier: PA2827787696
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 976200
ClinVar RCV Id: RCV001253422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Pro358Ala
CA349071329
NM_001353960.2:c.1072C>G