Canonical Allele Identifier: PA2828473851
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 423344
ClinVar RCV Id: RCV000480354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Val208Met
CA16617260
NM_001371247.1:c.622G>A