Canonical Allele Identifier: PA2827771868
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1519829
ClinVar RCV Id: RCV002043796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Asn1736Lys
CA349068416
NM_001353951.2:c.5208C>A
CA349068418
NM_001353951.2:c.5208C>G