Canonical Allele Identifier: PA2828471570
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 130219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Lys908Arg
CA155058
NM_001371246.1:c.2723A>G