Canonical Allele Identifier: PA112095
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4869
ClinVar RCV Id: RCV000005145 RCV000987342
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Tyr258Asn
CA117108
NM_023067.4:c.772T>A