Canonical Allele Identifier: PA2828474055
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 207044
ClinVar RCV Id: RCV000189198 RCV001857652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Asn297Ser
CA318089
NM_001371247.1:c.890A>G