Allele Registry

Canonical Allele Identifier: PA2826926637

Gene: FANCM HGNC NCBI

ClinVar Allele:

642375

ClinVar RCV:

RCV000818077

RCV002478909

RCV003226984

ClinVar Variation:

660798

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295063.1:p.Arg313Cys	CA7168893 NM_001308134.2:c.937C>T