Canonical Allele Identifier: PA2826013300
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 3067140
ClinVar RCV Id: RCV003992829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Phe1387Ile
CA349049950
NM_001165964.3:c.4159T>A