Canonical Allele Identifier: PA1139742036
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 840602
ClinVar RCV Id: RCV001042638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Asn298Asp
CA1939710
NM_021007.3:c.892A>G