Allele Registry

Canonical Allele Identifier: PA2826924955

Gene: FANCM HGNC NCBI

ClinVar Allele:

337894

ClinVar RCV:

RCV000383479

RCV000484209

RCV000763929

RCV001292951

RCV002255361

RCV004537776

ClinVar Variation:

313199

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295062.1:p.Leu500Val	CA7169086 NM_001308133.2:c.1498C>G