Canonical Allele Identifier: PA2828473598
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 521180
ClinVar RCV Id: RCV000622964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Ala34Val
CA349009970
NM_001371247.1:c.101C>T