Allele Registry

Canonical Allele Identifier: PA658660880

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000567655

RCV000630828

RCV002293461

ClinVar Variation:

485551

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Pro541Leu	CA374104406 NM_000136.3:c.1622C>T