Canonical Allele Identifier: PA2827773645
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 372977
ClinVar RCV Id: RCV000413641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Leu970Ile
CA16042438
NM_001353952.2:c.2908C>A