Canonical Allele Identifier: PA2499257830
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1213302
ClinVar RCV Id: RCV001591474 RCV002476892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001444.2:p.Pro140Ser
CA3614756
NM_001453.3:c.418C>T