Allele Registry

Canonical Allele Identifier: PA916006927

Gene: FANCC HGNC NCBI

ClinVar Allele:

459725

2419806

ClinVar RCV:

RCV000527037

RCV002051864

RCV002358436

RCV003221315

ClinVar Variation:

456164

2446385

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Asp197Glu	CA374109706 NM_001243744.2:c.591C>G CA374109707 NM_001243744.2:c.591C>A