Canonical Allele Identifier: PA2826011957
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1718669
ClinVar RCV Id: RCV002299994
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Phe402Cys
CA349070984
NM_001165964.3:c.1205T>G