Canonical Allele Identifier: PA2827783189
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1310724
ClinVar RCV Id: RCV001767838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Ala1378Asp
CA349050012
NM_001353957.2:c.4133C>A