Canonical Allele Identifier: PA2826011305
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1709553
ClinVar RCV Id: RCV002289368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala2006Thr
CA349062910
NM_001165963.4:c.6016G>A