Allele Registry

Canonical Allele Identifier: PA144132

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000049443

ClinVar Variation:

56034

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Asp224Val	CA144130 NM_000145.4:c.671A>T