Canonical Allele Identifier: PA111892
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4871
ClinVar RCV Id: RCV000005147 RCV000192031 RCV002251877 RCV003546451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Gly187Asp
CA117109
NM_023067.4:c.560G>A