Allele Registry

Canonical Allele Identifier: PA126293

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000017630

ClinVar Variation:

16243

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Ala163Val	CA126291 NM_181446.3:c.488C>T