Allele Registry

Canonical Allele Identifier: PA126328

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017640

ClinVar Variation:

16252

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Thr423Ala	CA126326 NM_181446.3:c.1267A>G