Canonical Allele Identifier: PA2826011108
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2430626
ClinVar RCV Id: RCV003129159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Lys1814Asn
CA349067542
NM_001165963.4:c.5442G>T
CA349067544
NM_001165963.4:c.5442G>C