Canonical Allele Identifier: PA2825354362
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 464902
ClinVar RCV Id: RCV000713068 RCV001078766
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Arg524Gln
CA1939839
NM_001040142.2:c.1571G>A