Canonical Allele Identifier: PA916055966
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 12881
ClinVar RCV Id: RCV000013741 RCV001217344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Leu1003Ile
CA122775
NM_021007.3:c.3007C>A