Canonical Allele Identifier: PA2825359946
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2923538
ClinVar RCV Id: RCV003783096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Phe1476Leu
CA349034275
NM_001040143.2:c.4426T>C
CA349034303
NM_001040143.2:c.4428C>A
CA349034305
NM_001040143.2:c.4428C>G