Canonical Allele Identifier: PA2826010547
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 853086
ClinVar RCV Id: RCV001057828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Met1533Lys
CA349072346
NM_001165963.4:c.4598T>A