Canonical Allele Identifier: PA2826014235
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2959868
ClinVar RCV Id: RCV003812043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Asp1930Asn
CA349063399
NM_001165964.3:c.5788G>A