Allele Registry

Canonical Allele Identifier: PA645431473

Gene: FANCM HGNC NCBI

ClinVar Allele:

329374

ClinVar RCV:

RCV000402989

RCV001030549

RCV002256202

RCV003229827

RCV004544559

ClinVar Variation:

313221

HGVS (amino-acid)	Matching Registered Transcripts
NP_065988.1:p.Arg1570His	CA7169843 NM_020937.4:c.4709G>A