Allele Registry

Canonical Allele Identifier: PA126301

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017632

ClinVar Variation:

16245

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Arg573Cys	CA126298 NM_000145.4:c.1717C>T