Allele Registry

Canonical Allele Identifier: PA126333

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017641

ClinVar Variation:

16253

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Ile545Thr	CA126330 NM_000145.4:c.1634T>C