Allele Registry

Canonical Allele Identifier: PA126297

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017631

RCV000431545

RCV001143060

ClinVar Variation:

16244

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Ile160Thr	CA126295 NM_000145.4:c.479T>C