Canonical Allele Identifier: PA2828472702
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 207011
ClinVar RCV Id: RCV000189163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Asn1544Asp
CA317994
NM_001371246.1:c.4630A>G