Allele Registry

Canonical Allele Identifier: PA658660568

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000567484

RCV000630855

RCV001788294

RCV002476246

ClinVar Variation:

485544

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Arg179Gln	CA5137696 NM_000136.3:c.536G>A