Canonical Allele Identifier: PA2827784133
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 451274

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.[Asn1924Ile;Leu1926del]
CA658657091
NM_001353957.2:c.5771_5773del