Allele Registry

Canonical Allele Identifier: PA126308

Gene: FSHR HGNC NCBI

ClinVar Allele:

31286

ClinVar RCV:

RCV000017635

RCV000252781

RCV000316299

RCV001711073

ClinVar Variation:

16247

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Ser654Asn	CA126306 NM_181446.3:c.1961G>A