Allele Registry

Canonical Allele Identifier: PA2826926351

Gene: FANCM HGNC NCBI

ClinVar Allele:

464041

ClinVar RCV:

RCV000554625

RCV000763926

RCV000989207

RCV001770408

RCV001821483

RCV003338648

ClinVar Variation:

456276

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295063.1:p.Arg18Gln	CA7168688 NM_001308134.2:c.53G>A