Allele Registry

Canonical Allele Identifier: PA645407672

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000413714

RCV001194630

RCV002523951

ClinVar Variation:

373364

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Met925Thr	CA16042355 NM_021007.3:c.2774T>C