Canonical Allele Identifier: PA111967
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369905
ClinVar RCV Id: RCV000408833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Leu106Phe
CA10654890
NM_023067.4:c.316C>T