Canonical Allele Identifier: PA2825355820
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 596677
ClinVar RCV Id: RCV000732587
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Ala1263Val
CA349028158
NM_001040142.2:c.3788C>T