Allele Registry

Canonical Allele Identifier: PA128571

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000022553

ClinVar Variation:

29704

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Pro587His	CA128569 NM_000145.4:c.1760C>A