Canonical Allele Identifier: PA2827769779
Gene: SCN1A HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ala342Glu
CA10602709
NM_001353951.2:c.1025C>A