Canonical Allele Identifier: PA2580447689
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2257521
ClinVar RCV Id: RCV002792444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Gly313Arg
CA83969674
NM_023067.4:c.937G>A
CA354701723
NM_023067.4:c.937G>C