Allele Registry

Canonical Allele Identifier: PA111901

Gene: FOXL2 HGNC NCBI

ClinVar RCV:

RCV000408824

ClinVar Variation:

369902

HGVS (amino-acid)	Matching Registered Transcripts
NP_075555.1:p.His104Arg	CA10654892 NM_023067.4:c.311A>G