Allele Registry

Canonical Allele Identifier: PA144126

Gene: FSHR HGNC NCBI

ClinVar RCV:

RCV000049441

ClinVar Variation:

56032

HGVS (amino-acid)	Matching Registered Transcripts
NP_000136.2:p.Leu601Val	CA144124 NM_000145.4:c.1801C>G