Canonical Allele Identifier: PA2827780256
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 372903
ClinVar RCV Id: RCV000414265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Gln1415Leu
CA16042437
NM_001353955.2:c.4244A>T