Allele Registry

Canonical Allele Identifier: PA658660582

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000527037

RCV002051864

RCV002358436

RCV003221315

ClinVar Variation:

456164

2446385

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Asp197Glu	CA374109706 NM_000136.3:c.591C>G CA374109707 NM_000136.3:c.591C>A