Canonical Allele Identifier: PA2826011668
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 805385
ClinVar RCV Id: RCV000992883
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Asp249Val
CA349073631
NM_001165964.3:c.746A>T