Canonical Allele Identifier: PA2826010352
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 856106
ClinVar RCV Id: RCV001061500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Phe1415Ser
CA349049945
NM_001165963.4:c.4244T>C