Canonical Allele Identifier: PA2825358078
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1063573
ClinVar RCV Id: RCV001373423 RCV001820078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Thr306Ser
CA1939713
NM_001040143.2:c.916A>T
CA349018603
NM_001040143.2:c.917C>G