Canonical Allele Identifier: PA2826013954
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 427080
ClinVar RCV Id: RCV000489093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Met1752Val
CA349068113
NM_001165964.3:c.5254A>G