Canonical Allele Identifier: PA913201600
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 593636
ClinVar RCV Id: RCV000728735
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Tyr1274Cys
CA349054188
NM_001165963.4:c.3821A>G