Canonical Allele Identifier: PA2827778588
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 805385
ClinVar RCV Id: RCV000992883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Asp249Val
CA349073631
NM_001353955.2:c.746A>T