Allele Registry

Canonical Allele Identifier: PA126300

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017632

ClinVar Variation:

16245

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Arg547Cys	CA126298 NM_181446.3:c.1639C>T