Canonical Allele Identifier: PA2830015065
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3096484
ClinVar RCV Id: RCV004392354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Pro332Leu
CA354701222
NM_023067.4:c.995C>T