Canonical Allele Identifier: PA2827788956
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1203729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ala1282Val
CA349053215
NM_001353960.2:c.3845C>T