Allele Registry

Canonical Allele Identifier: PA916006559

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000115342

RCV000709080

RCV000805530

RCV001011247

RCV003492471

ClinVar Variation:

127532

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230672.1:p.Arg458Ser	CA287187 NM_001243743.2:c.1374A>C CA374106209 NM_001243743.2:c.1374A>T