Canonical Allele Identifier: PA2827780901
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 374394
ClinVar RCV Id: RCV000414903
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Val1772Ala
CA16043651
NM_001353955.2:c.5315T>C