Allele Registry

Canonical Allele Identifier: PA658800341

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000630907

RCV001017222

ClinVar Variation:

526383

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Arg361Gln	CA5137460 NM_000136.3:c.1082G>A