Canonical Allele Identifier: PA318059
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 207032
ClinVar RCV Id: RCV000713078 RCV001079374 RCV002314756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Ala24Thr
CA318057
NM_021007.3:c.70G>A