Allele Registry

Canonical Allele Identifier: PA658800292

Gene: FANCC HGNC NCBI

ClinVar RCV:

RCV000630906

RCV003162794

RCV003238790

ClinVar Variation:

526382

HGVS (amino-acid)	Matching Registered Transcripts
NP_000127.2:p.Met16Leu	CA374340454 NM_000136.3:c.46A>T CA374340458 NM_000136.3:c.46A>C