Canonical Allele Identifier: PA2827786058
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189990

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Leu1324Pro
CA303491
NM_001353958.2:c.3971T>C