Canonical Allele Identifier: PA2827786489
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 375515
ClinVar RCV Id: RCV000417022
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Asn1577Ile
CA16044312
NM_001353958.2:c.4730A>T