Allele Registry

Canonical Allele Identifier: PA2825883094

Gene: NR2F2 HGNC NCBI

ClinVar RCV:

RCV000116200

ClinVar Variation:

128233

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138628.1:p.Asn52Ile	CA151540 NM_001145156.1:c.155A>T