Allele Registry

Canonical Allele Identifier: PA916006929

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000479725

RCV002356770

RCV002481504

ClinVar Variation:

419075

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Asp197Val	CA16618887 NM_001243744.2:c.590A>T