Canonical Allele Identifier: PA645392763
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369896
ClinVar RCV Id: RCV000408808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Ala86Pro
CA10654898
NM_023067.4:c.256G>C