Allele Registry

Canonical Allele Identifier: PA645431440

Gene: FANCM HGNC NCBI

ClinVar Variation Id: 313218

HGVS (amino-acid)	Matching Registered Transcripts
NP_065988.1:p.Arg1456Cys	CA7169707 NM_020937.4:c.4366C>T