Allele Registry

Canonical Allele Identifier: PA2828470697

Gene: SCN2A HGNC NCBI

ClinVar Allele:

628771

ClinVar RCV:

RCV000819241

ClinVar Variation:

661756

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Asp343Gly	CA349019879 NM_001371246.1:c.1028A>G