Canonical Allele Identifier: PA2826012714
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 580287
ClinVar RCV Id: RCV000703775
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Asn971Lys
CA349060463
NM_001165964.3:c.2913C>G
CA349060465
NM_001165964.3:c.2913C>A