Allele Registry

Canonical Allele Identifier: PA144120

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000049439

ClinVar Variation:

56030

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Pro348Arg	CA144118 NM_000145.4:c.1043C>G