Canonical Allele Identifier: PA2825359145
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 994949
ClinVar RCV Id: RCV001288733
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Ala980Gly
CA349019403
NM_001040143.2:c.2939C>G