Canonical Allele Identifier: PA2827788731
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 805382
ClinVar RCV Id: RCV000992879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Val1140Ala
CA349056680
NM_001353960.2:c.3419T>C