Canonical Allele Identifier: PA303325
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Leu897Ser
CA303322
NM_001165963.4:c.2690T>C