Canonical Allele Identifier: PA2826011277
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2959868
ClinVar RCV Id: RCV003812043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Asp1958Asn
CA349063399
NM_001165963.4:c.5872G>A