Allele Registry

Canonical Allele Identifier: PA891847680

Gene: FANCM HGNC NCBI

ClinVar Variation Id: 565803

HGVS (amino-acid)	Matching Registered Transcripts
NP_065988.1:p.Gln522Arg	CA7169083 NM_020937.4:c.1565A>G