ClinGen Allele Registry
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Canonical Allele Identifier:
PA111901
Gene: FOXL2
HGNC
NCBI
Linked Data
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_075555.1:p.His104Arg
NM_023067.4:c.311A>G