Allele Registry

Canonical Allele Identifier: PA126309

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017635

RCV000252781

RCV000316299

RCV001711073

ClinVar Variation:

16247

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Ser680Asn	CA126306 NM_000145.4:c.2039G>A