Allele Registry

Canonical Allele Identifier: PA2826926036

Gene: FANCM HGNC NCBI

ClinVar Allele:

320604

ClinVar RCV:

RCV000367982

RCV000658691

ClinVar Variation:

313225

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295062.1:p.His1677Arg	CA7169910 NM_001308133.2:c.5030A>G