Allele Registry

Canonical Allele Identifier: PA126329

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017640

ClinVar Variation:

16252

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Thr449Ala	CA126326 NM_000145.4:c.1345A>G