Canonical Allele Identifier: PA645392772
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369904
ClinVar RCV Id: RCV000408788
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Asn105_Leu106del
CA10654889
NM_023067.4:c.314_319del