Allele Registry

Canonical Allele Identifier: PA1139700439

Gene: FOXC1 HGNC NCBI

ClinVar RCV:

RCV001198073

ClinVar Variation:

931490

HGVS (amino-acid)	Matching Registered Transcripts
NP_001444.2:p.Trp152Cys	CA362558862 NM_001453.3:c.456G>C CA362558863 NM_001453.3:c.456G>T