Allele Registry

Canonical Allele Identifier: PA126321

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017638

ClinVar Variation:

16250

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Asp567Asn	CA126318 NM_000145.4:c.1699G>A