Allele Registry

Canonical Allele Identifier: PA126320

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017638

ClinVar Variation:

16250

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Asp541Asn	CA126318 NM_181446.3:c.1621G>A