Canonical Allele Identifier: PA2826013149
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 571695
ClinVar RCV Id: RCV000692909
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Phe1302Ser
CA349052909
NM_001165964.3:c.3905T>C