Canonical Allele Identifier: PA2827789016
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 488378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ile1318Asn
CA349050737
NM_001353960.2:c.3953T>A