Allele Registry

Canonical Allele Identifier: PA126317

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017637

ClinVar Variation:

16249

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Thr449Ile	CA126314 NM_000145.4:c.1346C>T