Canonical Allele Identifier: PA210023
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 194555
ClinVar RCV Id: RCV000174944 RCV000197677 RCV000515237 RCV001265273 RCV001847809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Arg853Gln
CA210022
NM_021007.3:c.2558G>A