Canonical Allele Identifier: PA2827784481
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 801821
ClinVar RCV Id: RCV000986915
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Val212Ala
CA1943470
NM_001353958.2:c.635T>C