Canonical Allele Identifier: PA2825359703
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 206991
ClinVar RCV Id: RCV000189141 RCV000416964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Ala1316Val
CA317939
NM_001040143.2:c.3947C>T