Allele Registry

Canonical Allele Identifier: PA658661718

Gene: FANCM HGNC NCBI

ClinVar Variation Id: 456259

HGVS (amino-acid)	Matching Registered Transcripts
NP_065988.1:p.Tyr777Cys	CA7169337 NM_020937.4:c.2330A>G