Canonical Allele Identifier: PA2825356737
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2580446
ClinVar RCV Id: RCV003329641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Ser1556Thr
CA349036432
NM_001040142.2:c.4667G>C