Canonical Allele Identifier: PA2826010357
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 986202
ClinVar RCV Id: RCV001267495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Asn1417Ile
CA349049929
NM_001165963.4:c.4250A>T