Allele Registry

Canonical Allele Identifier: PA126316

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017637

ClinVar Variation:

16249

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Thr423Ile	CA126314 NM_181446.3:c.1268C>T