Canonical Allele Identifier: PA2825353521
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 586499
ClinVar RCV Id: RCV000713077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Leu210Arg
CA349017374
NM_001040142.2:c.629T>G