Canonical Allele Identifier: PA645392774
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369906
ClinVar RCV Id: RCV000408897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Ser107Gly
CA10654888
NM_023067.4:c.319A>G