Canonical Allele Identifier: PA2827776299
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1012964
ClinVar RCV Id: RCV001311219
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Val767Ala
CA349064175
NM_001353954.2:c.2300T>C