Canonical Allele Identifier: PA2827777469
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 853086
ClinVar RCV Id: RCV001057828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Met1521Lys
CA349072346
NM_001353954.2:c.4562T>A