Allele Registry

Canonical Allele Identifier: PA126332

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017641

ClinVar Variation:

16253

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Ile519Thr	CA126330 NM_181446.3:c.1556T>C