Canonical Allele Identifier: PA159868
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134454
ClinVar RCV Id: RCV000121136 RCV001657762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Arg349Gly
CA159867
NM_023067.4:c.1045C>G