Canonical Allele Identifier: PA303391
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189952
ClinVar RCV Id: RCV000180905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ala1328Val
CA303389
NM_006920.6:c.3983C>T