Canonical Allele Identifier: PA2826011601
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1479129
ClinVar RCV Id: RCV001976629
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Asn211Thr
CA349074294
NM_001165964.3:c.632A>C