Allele Registry

Canonical Allele Identifier: PA1139725489

Gene: SCN2A HGNC NCBI

ClinVar Allele:

825079

ClinVar RCV:

RCV001041043

ClinVar Variation:

839313

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Thr1212Pro	CA349026266 NM_021007.3:c.3634A>C