Canonical Allele Identifier: PA2827780235
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 3067140
ClinVar RCV Id: RCV003992829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Phe1403Ile
CA349049950
NM_001353955.2:c.4207T>A