Canonical Allele Identifier: PA2827789139
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1705490
ClinVar RCV Id: RCV002283804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Phe1386Cys
CA349049947
NM_001353960.2:c.4157T>G