Canonical Allele Identifier: PA2825356700
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2949506
ClinVar RCV Id: RCV003804672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Asp1554Tyr
CA349036405
NM_001040142.2:c.4660G>T