Canonical Allele Identifier: PA2828470679
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 589983
ClinVar RCV Id: RCV002318168 RCV002533055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Asn308Ser
CA1939714
NM_001371246.1:c.923A>G