Canonical Allele Identifier: PA2499275253
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1189857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Lys547Asn
CA1943282
NM_006920.6:c.1641G>T
CA349069050
NM_006920.6:c.1641G>C