Canonical Allele Identifier: PA658660986
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 464902
ClinVar RCV Id: RCV000713068 RCV001078766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Arg524Gln
CA1939839
NM_021007.3:c.1571G>A