Canonical Allele Identifier: PA2741883994
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2629736
ClinVar RCV Id: RCV003399860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001444.2:p.Cys135Tyr
CA362558744
NM_001453.3:c.404G>A