Canonical Allele Identifier: PA1139741997
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 934399
ClinVar RCV Id: RCV001202780 RCV003163525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Leu210Gln
CA349017376
NM_021007.3:c.629T>A