Allele Registry

Canonical Allele Identifier: PA2826924757

Gene: FANCM HGNC NCBI

ClinVar RCV:

RCV000353097

RCV001706480

RCV002258875

RCV004544556

ClinVar Variation:

313196

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295062.1:p.Glu283Ala	CA7168890 NM_001308133.2:c.848A>C