Canonical Allele Identifier: PA2826010135
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2430162
ClinVar RCV Id: RCV003128168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Leu1265Met
CA349054328
NM_001165963.4:c.3793C>A