Canonical Allele Identifier: PA2580447674
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2031098
ClinVar RCV Id: RCV002872196
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Val245Gly
CA354703945
NM_023067.4:c.734T>G