Canonical Allele Identifier: PA2827787780
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1365578
ClinVar RCV Id: RCV001961854

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ala395Val
CA1943338
NM_001353960.2:c.1184C>T