Canonical Allele Identifier: PA2827760383
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 202173
ClinVar RCV Id: RCV000986878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Ile1471Leu
CA275462
NM_001353949.2:c.4411A>C