Canonical Allele Identifier: PA112024
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369899
ClinVar RCV Id: RCV000408814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Ser101Arg
CA10654895
NM_023067.4:c.303C>G
CA354706889
NM_023067.4:c.303C>A
CA354706911
NM_023067.4:c.301A>C