Canonical Allele Identifier: PA2825359945
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1804532
ClinVar RCV Id: RCV002469833 RCV002573599
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Asn1475Lys
CA349034269
NM_001040143.2:c.4425C>A
CA349034271
NM_001040143.2:c.4425C>G