Canonical Allele Identifier: PA2825358897
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 212125
ClinVar RCV Id: RCV000193985 RCV000413708 RCV001265401 RCV001390104
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Arg856Gln
CA207842
NM_001040143.2:c.2567G>A