Allele Registry

Canonical Allele Identifier: PA2826924795

Gene: FANCM HGNC NCBI

ClinVar Allele:

241832

ClinVar RCV:

RCV000233464

RCV001570689

RCV001820757

RCV002255337

ClinVar Variation:

241314

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295062.1:p.Pro321Leu	CA7168910 NM_001308133.2:c.962C>T