Allele Registry

Canonical Allele Identifier: PA339014

Gene: FANCC HGNC NCBI

ClinVar Allele:

212673

ClinVar RCV:

RCV000199976

RCV000520121

RCV001012322

RCV001167954

RCV003153471

ClinVar Variation:

216285

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Arg532Lys	CA339012 NM_000136.3:c.1595G>A