Canonical Allele Identifier: PA317896
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 206975
ClinVar RCV Id: RCV001852499 RCV001721217 RCV002492872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Gly899Asp
CA317895
NM_001040142.2:c.2696G>A