Canonical Allele Identifier: PA645392757
Gene: FOXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 369892
ClinVar RCV Id: RCV000408759 RCV003678999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_075555.1:p.Met65Ile
CA10654903
NM_023067.4:c.195G>A
CA354707411
NM_023067.4:c.195G>T
CA354707414
NM_023067.4:c.195G>C