Canonical Allele Identifier: PA318198
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 207084
ClinVar RCV Id: RCV000189239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Asp1554Gly
CA318196
NM_021007.3:c.4661A>G