Canonical Allele Identifier: PA2827775383
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2796440
ClinVar RCV Id: RCV003753904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Ile110Asn
CA349077031
NM_001353954.2:c.329T>A