Allele Registry

Canonical Allele Identifier: PA126336

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017642

ClinVar Variation:

16254

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Ser128Tyr	CA126334 NM_000145.4:c.383C>A