Canonical Allele Identifier: PA2573208262
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1344729
ClinVar RCV Id: RCV001849730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001444.2:p.Lys145del
CA3614759
NM_001453.3:c.433_435del