Canonical Allele Identifier: PA2826010378
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 836631
ClinVar RCV Id: RCV001037807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Lys1432Ile
CA349049621
NM_001165963.4:c.4295A>T