Canonical Allele Identifier: PA303548
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190011
ClinVar RCV Id: RCV000180967 RCV002316981
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ala1662Val
CA303545
NM_001165963.4:c.4985C>T