Canonical Allele Identifier: PA2827777436
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 69406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Ser1504Leu
CA357173
NM_001353954.2:c.4511C>T