Allele Registry

Canonical Allele Identifier: PA645438742

Gene: FANCG HGNC NCBI

ClinVar RCV:

RCV000234010

RCV001833247

ClinVar Variation:

239966

HGVS (amino-acid)	Matching Registered Transcripts
NP_004620.1:p.Arg98Gln	CA5040093 NM_004629.2:c.293G>A