Allele Registry

Canonical Allele Identifier: PA2826926077

Gene: FANCM HGNC NCBI

ClinVar RCV:

RCV000231642

RCV000253417

RCV000658692

RCV001331161

RCV002257595

ClinVar Variation:

241324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295062.1:p.Ile1716Val	CA7169934 NM_001308133.2:c.5146A>G