Canonical Allele Identifier: PA645392788
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369920
ClinVar RCV Id: RCV000408834
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Ala216Val
CA10654875
NM_023067.4:c.647C>T