Canonical Allele Identifier: PA2580447686
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2255427
ClinVar RCV Id: RCV002772315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Val270Leu
CA354703368
NM_023067.4:c.808G>T
CA354703371
NM_023067.4:c.808G>C