Canonical Allele Identifier: PA2826012979
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1475150
ClinVar RCV Id: RCV001973907 RCV003136396
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Phe1198Val
CA349055801
NM_001165964.3:c.3592T>G