Allele Registry

Canonical Allele Identifier: PA645431412

Gene: FANCM HGNC NCBI

Linked Data

ClinVar RCV:

RCV000475344

RCV000989208

RCV001569551

RCV001821346

RCV002257746

RCV003316605

RCV003447530

RCV004535465

ClinVar Variation:

414849

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_065988.1:p.Arg1099His	CA7169492 NM_020937.4:c.3296G>A