Canonical Allele Identifier: PA2827789754
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2057676
ClinVar RCV Id: RCV002942053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Pro1730Leu
CA349068303
NM_001353960.2:c.5189C>T