Canonical Allele Identifier: PA2828470411
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 422127
ClinVar RCV Id: RCV000484885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Arg102Gln
CA16617256
NM_001371246.1:c.305G>A