Canonical Allele Identifier: PA2826012344
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Pro740Leu
CA303333
NM_001165964.3:c.2219C>T