Allele Registry

Canonical Allele Identifier: PA2826924858

Gene: FANCM HGNC NCBI

ClinVar RCV:

RCV001071165

RCV001292690

RCV001732036

RCV002505660

ClinVar Variation:

864066

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295062.1:p.Glu391Gln	CA7168977 NM_001308133.2:c.1171G>C