Canonical Allele Identifier: PA1139714443
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 958033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Asn86Ser
CA60270523
NM_006920.6:c.257A>G