Canonical Allele Identifier: PA2825353509
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 423904
ClinVar RCV Id: RCV000484447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Phe207Cys
CA16617259
NM_001040142.2:c.620T>G