Canonical Allele Identifier: PA2499287628
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1214913
ClinVar RCV Id: RCV001593388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Arg1235Gln
CA349027638
NM_021007.3:c.3704G>A