Allele Registry

Canonical Allele Identifier: PA126294

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017630

ClinVar Variation:

16243

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Ala189Val	CA126291 NM_000145.4:c.566C>T