Canonical Allele Identifier: PA2829675942
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1310724
ClinVar RCV Id: RCV001767838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ala1395Asp
CA349050012
NM_006920.6:c.4184C>A