Canonical Allele Identifier: PA2827778909
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189920
ClinVar RCV Id: RCV000180872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Val422Ala
CA303306
NM_001353955.2:c.1265T>C