Allele Registry

Canonical Allele Identifier: PA2830358089

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000049443

ClinVar Variation:

56034

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Asp198Val	CA144130 NM_181446.3:c.593A>T