Allele Registry

Canonical Allele Identifier: PA2825883127

Gene: NR2F2 HGNC NCBI

ClinVar RCV:

RCV000116199

RCV000494657

RCV001729389

ClinVar Variation:

128232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138628.1:p.Ser188Tyr	CA151538 NM_001145156.1:c.563C>A