Allele Registry

Canonical Allele Identifier: PA2826924650

Gene: FANCM HGNC NCBI

ClinVar Allele:

399799

ClinVar RCV:

RCV000463663

RCV001555524

RCV002256303

RCV004541481

ClinVar Variation:

414850

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295062.1:p.His164Pro	CA7168773 NM_001308133.2:c.491A>C