Allele Registry

Canonical Allele Identifier: PA2826926878

Gene: FANCM HGNC NCBI

ClinVar Allele:

320553

ClinVar RCV:

RCV000269296

RCV000763930

RCV001030474

RCV001292875

RCV001590938

RCV004537777

ClinVar Variation:

313200

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295063.1:p.Arg581Cys	CA7169137 NM_001308134.2:c.1741C>T