Canonical Allele Identifier: PA2827781163
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Ile1943Met
CA317108
NM_001353955.2:c.5829A>G