Allele Registry

Canonical Allele Identifier: PA658661710

Gene: FANCM HGNC NCBI

ClinVar Variation Id: 456258

HGVS (amino-acid)	Matching Registered Transcripts
NP_065988.1:p.Arg666Gly	CA7169200 NM_020937.4:c.1996A>G