Canonical Allele Identifier: PA2827780722
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2823831
ClinVar RCV Id: RCV003754330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Asn1679Ser
CA1942697
NM_001353955.2:c.5036A>G