Canonical Allele Identifier: PA2827766142
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_001340879.1:p.Tyr1263Cys
CA349054188
NM_001353950.2:c.3788A>G