Canonical Allele Identifier: PA2827755879
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 958033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Asn86Ser
CA60270523
NM_001353949.2:c.257A>G