Allele Registry

Canonical Allele Identifier: PA151541

Gene: NR2F2 HGNC NCBI

ClinVar RCV:

RCV000116200

ClinVar Variation:

128233

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138627.1:p.Asn72Ile	CA151540 NM_001145155.2:c.215A>T