Canonical Allele Identifier: PA2826009476
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1186442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ser643Asn
CA1943230
NM_001165963.4:c.1928G>A