Canonical Allele Identifier: PA2825356644
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2662917
ClinVar RCV Id: RCV003441582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Cys1542Ser
CA349036311
NM_001040142.2:c.4624T>A
CA349036313
NM_001040142.2:c.4625G>C