Allele Registry

Canonical Allele Identifier: PA1139737285

Gene: FANCM HGNC NCBI

ClinVar RCV:

RCV001071165

RCV001292690

RCV001732036

RCV002505660

ClinVar Variation:

864066

HGVS (amino-acid)	Matching Registered Transcripts
NP_065988.1:p.Glu417Gln	CA7168977 NM_020937.4:c.1249G>C