Allele Registry

Canonical Allele Identifier: PA104936

Gene: CFP HGNC NCBI

ClinVar RCV:

RCV000011933

ClinVar Variation:

11183

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138724.1:p.Gly298Val	CA121398 NM_001145252.3:c.893G>T