Canonical Allele Identifier: PA2826014229
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ile1927Met
CA317108
NM_001165964.3:c.5781A>G