Canonical Allele Identifier: PA2580447526
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2295040
ClinVar RCV Id: RCV002868303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Gly37Asp
CA2639813
NM_023067.4:c.110G>A