Canonical Allele Identifier: PA2826013521
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 853086
ClinVar RCV Id: RCV001057828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Met1505Lys
CA349072346
NM_001165964.3:c.4514T>A