Canonical Allele Identifier: PA2580447690
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2361547
ClinVar RCV Id: RCV002984021
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Pro332Ala
CA2639705
NM_023067.4:c.994C>G