Canonical Allele Identifier: PA094553
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1497461
ClinVar RCV Id: RCV001996092 RCV002319742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Thr1623Asn
CA349037646
NM_001040142.2:c.4868C>A