Canonical Allele Identifier: PA2826011927
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1013695
ClinVar RCV Id: RCV001312320
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Thr391Ser
CA349071050
NM_001165964.3:c.1171A>T