Allele Registry

Canonical Allele Identifier: PA126304

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017633

RCV000252249

RCV000299214

RCV000356409

RCV001636603

ClinVar Variation:

16246

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Ala281Thr	CA126302 NM_181446.3:c.841G>A