Allele Registry

Canonical Allele Identifier: PA2829361130

Gene: CFD HGNC NCBI

ClinVar Allele:

624673

ClinVar RCV:

RCV000788228

ClinVar Variation:

636410

HGVS (amino-acid)	Matching Registered Transcripts
NP_001919.2:p.Ser42Leu	CA402920654 NM_001928.4:c.125C>T