Canonical Allele Identifier: PA2826011299
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 660951
ClinVar RCV Id: RCV000818256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.His1997Arg
CA349063024
NM_001165963.4:c.5990A>G