Canonical Allele Identifier: PA2828470419
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1010462
ClinVar RCV Id: RCV001308099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Asn116Ser
CA349011765
NM_001371246.1:c.347A>G