Canonical Allele Identifier: PA2826012239
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1014248
ClinVar RCV Id: RCV001312958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Val645Leu
CA1943228
NM_001165964.3:c.1933G>T
CA349067260
NM_001165964.3:c.1933G>C