Allele Registry

Canonical Allele Identifier: PA128990

Gene: FOXC1 HGNC NCBI

ClinVar RCV:

RCV000023070

RCV000153259

RCV000162086

RCV001087974

ClinVar Variation:

30156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001444.2:p.Pro297Ser	CA128989 NM_001453.3:c.889C>T