Canonical Allele Identifier: PA645407743
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 12877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Leu1563Val
CA122769
NM_021007.3:c.4687C>G