Allele Registry

Canonical Allele Identifier: PA2826925807

Gene: FANCM HGNC NCBI

ClinVar Variation Id: 313218

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295062.1:p.Arg1430Cys	CA7169707 NM_001308133.2:c.4288C>T