Canonical Allele Identifier: PA2499289726
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1255995
ClinVar RCV Id: RCV001661755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Ser263Arg
CA354703578
NM_023067.4:c.789C>G
CA354703588
NM_023067.4:c.789C>A
CA354703598
NM_023067.4:c.787A>C