Allele Registry

Canonical Allele Identifier: PA107438

Gene: NR2F2 HGNC NCBI

ClinVar RCV:

RCV000116200

ClinVar Variation:

128233

HGVS (amino-acid)	Matching Registered Transcripts
NP_066285.1:p.Asn205Ile	CA151540 NM_021005.4:c.614A>T