Canonical Allele Identifier: PA916036567
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Ile1955Met
CA317108
NM_001353948.2:c.5865A>G