Allele Registry

Canonical Allele Identifier: PA121400

Gene: CFP HGNC NCBI

ClinVar RCV:

RCV000011933

ClinVar Variation:

11183

HGVS (amino-acid)	Matching Registered Transcripts
NP_002612.1:p.Gly298Val	CA121398 NM_002621.2:c.893G>T