Canonical Allele Identifier: PA2830015006
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4854
ClinVar RCV Id: RCV000005128 RCV000005127 RCV000408801 RCV002512795
ClinVar Variation Id: 4862
ClinVar RCV Id: RCV000005138 RCV002490318
ClinVar Variation Id: 369923
ClinVar RCV Id: RCV000408883 RCV002524615
ClinVar Variation Id: 369925
ClinVar RCV Id: RCV000408895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Ala225_Ala234dup