Allele Registry

Canonical Allele Identifier: PA916006978

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000231342

RCV001026618

RCV001274479

RCV001354988

RCV001551720

ClinVar Variation:

237076

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230673.1:p.Met254Val	CA5137637 NM_001243744.2:c.760A>G