Canonical Allele Identifier: PA2827777279
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2012859
ClinVar RCV Id: RCV002843428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Thr1418Ser
CA349049638
NM_001353954.2:c.4252A>T