Canonical Allele Identifier: PA2826013499
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Pro1491Thr
CA317497
NM_001165964.3:c.4471C>A