Canonical Allele Identifier: PA2825353662
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1317603
ClinVar RCV Id: RCV001768169 RCV001868718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Ser249Thr
CA349017918
NM_001040142.2:c.745T>A