Allele Registry

Canonical Allele Identifier: PA2826925091

Gene: FANCM HGNC NCBI

ClinVar Variation Id: 456258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295062.1:p.Arg640Gly	CA7169200 NM_001308133.2:c.1918A>G