Allele Registry

Canonical Allele Identifier: PA151539

Gene: NR2F2 HGNC NCBI

ClinVar RCV:

RCV000116199

RCV000494657

RCV001729389

ClinVar Variation:

128232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138627.1:p.Ser208Tyr	CA151538 NM_001145155.2:c.623C>A