Allele Registry

Canonical Allele Identifier: PA645407680

Gene: SCN2A HGNC NCBI

ClinVar Allele:

365811

ClinVar RCV:

RCV000438096

RCV001059949

RCV003483613

ClinVar Variation:

390480

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Asp997Gly	CA16603912 NM_021007.3:c.2990A>G