Allele Registry

Canonical Allele Identifier: PA891845153

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000709084

RCV001017185

RCV001825407

RCV003492140

ClinVar Variation:

584738

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Gln357Glu	CA5137482 NM_000136.3:c.1069C>G