Allele Registry

Canonical Allele Identifier: PA916022075

Gene: CFD HGNC NCBI

ClinVar Allele:

624673

ClinVar RCV:

RCV000788228

ClinVar Variation:

636410

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304264.1:p.Ser49Leu	CA402920654 NM_001317335.2:c.146C>T