Canonical Allele Identifier: PA2828472750
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 12877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Leu1563Val
CA122769
NM_001371246.1:c.4687C>G