Canonical Allele Identifier: PA2826008823
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2751140
ClinVar RCV Id: RCV003589476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Leu108Val
CA1943535
NM_001165963.4:c.322C>G