Canonical Allele Identifier: PA2827780250
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1321314
ClinVar RCV Id: RCV001779411
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Tyr1410Phe
CA349049898
NM_001353955.2:c.4229A>T