Allele Registry

Canonical Allele Identifier: PA2830358112

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000049439

ClinVar Variation:

56030

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Pro322Arg	CA144118 NM_181446.3:c.965C>G