Canonical Allele Identifier: PA2825358019
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1070304
ClinVar RCV Id: RCV001382401 RCV002319707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Ala263Thr
CA349018089
NM_001040143.2:c.787G>A