Allele Registry

Canonical Allele Identifier: PA2830358193

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000049441

ClinVar Variation:

56032

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Leu575Val	CA144124 NM_181446.3:c.1723C>G