Canonical Allele Identifier: PA916055747
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 801776
ClinVar RCV Id: RCV000986850 RCV002283516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Val213Ala
CA349017420
NM_021007.3:c.638T>C