Canonical Allele Identifier: PA645407702
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 379254
ClinVar RCV Id: RCV000444205 RCV001265495 RCV001252614 RCV001848749 RCV003989530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Arg1319Leu
CA16603920
NM_021007.3:c.3956G>T