Allele Registry

Canonical Allele Identifier: PA2826925200

Gene: FANCM HGNC NCBI

ClinVar RCV:

RCV000538182

RCV001088406

RCV004541644

ClinVar Variation:

456259

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295062.1:p.Tyr751Cys	CA7169337 NM_001308133.2:c.2252A>G