Canonical Allele Identifier: PA2825359450
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3026693
ClinVar RCV Id: RCV003887086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Lys1178Met
CA349025769
NM_001040143.2:c.3533A>T