Allele Registry

Canonical Allele Identifier: PA645431492

Gene: FANCM HGNC NCBI

ClinVar RCV:

RCV000367982

RCV000658691

ClinVar Variation:

313225

HGVS (amino-acid)	Matching Registered Transcripts
NP_065988.1:p.His1703Arg	CA7169910 NM_020937.4:c.5108A>G