Canonical Allele Identifier: PA658661038
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 464907
ClinVar RCV Id: RCV000551875 RCV001556515 RCV002265794 RCV002456120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Arg1177Trp
CA1940130
NM_021007.3:c.3529C>T