Allele Registry

Canonical Allele Identifier: PA2830358128

Gene: FSHR HGNC NCBI

ClinVar Variation Id: 336482

HGVS (amino-acid)	Matching Registered Transcripts
NP_852111.2:p.Ala418Thr	CA1653677 NM_181446.3:c.1252G>A