Canonical Allele Identifier: PA2741982189
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2541757
ClinVar RCV Id: RCV003256799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Leu277Pro
CA2639718
NM_023067.4:c.830T>C