ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825359950
Gene: SCN2A
HGNC
NCBI
Linked Data
ClinVar Variation Id:
842452
ClinVar RCV Id:
RCV001044878
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001035233.1:p.Gln1478Glu
CA349034330
NM_001040143.2:c.4432C>G