Allele Registry

Canonical Allele Identifier: PA144123

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000049440

ClinVar Variation:

56031

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Ala575Val	CA144121 NM_000145.4:c.1724C>T