Allele Registry

Canonical Allele Identifier: PA111958

Gene: FOXL2 HGNC NCBI

ClinVar RCV:

RCV000005139

RCV003894790

ClinVar Variation:

4863

HGVS (amino-acid)	Matching Registered Transcripts
NP_075555.1:p.Ile84Ser	CA210687 NM_023067.4:c.251T>G