Canonical Allele Identifier: PA2827773845
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 194721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Ala1150Thr
CA240854
NM_001353952.2:c.3448G>A