Allele Registry

Canonical Allele Identifier: PA299162

Gene: FANCC HGNC NCBI

ClinVar Allele:

180346

ClinVar RCV:

RCV000206295

RCV000586258

RCV001354181

RCV001549275

RCV002415701

RCV002498797

ClinVar Variation:

182477

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Ser264Arg	CA299160 NM_000136.3:c.792T>G CA374109277 NM_000136.3:c.792T>A CA374109282 NM_000136.3:c.790A>C