Canonical Allele Identifier: PA2825355727
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 422520
ClinVar RCV Id: RCV000479012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Val1215Phe
CA16617268
NM_001040142.2:c.3643G>T