Canonical Allele Identifier: PA221598
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Asn1528Lys
CA221595
NM_001165963.4:c.4584C>A
CA349072381
NM_001165963.4:c.4584C>G