Allele Registry

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Canonical Allele Identifier: PA2573095514

Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1318744

ClinVar RCV Id: RCV001768368 RCV002503252

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_075555.1:p.Ala234del	CA658822032 NM_023067.4:c.700_701insAGCGGCTGCAGCAGCTGCGGCTGCAGCCGC CA2577918194 NM_023067.4:c.696_698del