Canonical Allele Identifier: PA119642
Gene: FOXC1 HGNC NCBI
ClinVar RCV:
RCV000008979
ClinVar Variation:
8459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001444.2:p.Ile87Met
CA119641
NM_001453.3:c.261C>G