Allele Registry

Canonical Allele Identifier: PA2573094722

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV001777077

RCV003772129

ClinVar Variation:

1321098

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Gln1531His	CA349036240 NM_021007.3:c.4593A>T CA349036241 NM_021007.3:c.4593A>C