Allele Registry

Canonical Allele Identifier: PA107469

Gene: NR2F2 HGNC NCBI

ClinVar RCV:

RCV000116199

RCV000494657

RCV001729389

ClinVar Variation:

128232

HGVS (amino-acid)	Matching Registered Transcripts
NP_066285.1:p.Ser341Tyr	CA151538 NM_021005.4:c.1022C>A