Allele Registry

Canonical Allele Identifier: PA119635

Gene: FOXC1 HGNC NCBI

ClinVar RCV:

RCV000008969

ClinVar Variation:

8453

HGVS (amino-acid)	Matching Registered Transcripts
NP_001444.2:p.Ile126Met	CA119634 NM_001453.3:c.378C>G