Canonical Allele Identifier: PA1139724436
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 870196
ClinVar RCV Id: RCV001089735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Cys353Ser
CA349020364
NM_021007.3:c.1057T>A
CA349020373
NM_021007.3:c.1058G>C