Allele Registry

Canonical Allele Identifier: PA112095

Gene: FOXL2 HGNC NCBI

ClinVar RCV:

RCV000005145

RCV000987342

ClinVar Variation:

4869

HGVS (amino-acid)	Matching Registered Transcripts
NP_075555.1:p.Tyr258Asn	CA117108 NM_023067.4:c.772T>A