Canonical Allele Identifier: PA1139741270
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 839613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Glu884Lys
CA1942695
NM_001353961.2:c.2650G>A