Canonical Allele Identifier: PA2499287683
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 999441
ClinVar RCV Id: RCV001295439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Val1268Leu
CA349028242
NM_021007.3:c.3802G>T
CA349028243
NM_021007.3:c.3802G>C