Allele Registry

Canonical Allele Identifier: PA2826924935

Gene: FANCM HGNC NCBI

ClinVar Variation Id: 643944

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295062.1:p.Met480Ile	CA389592621 NM_001308133.2:c.1440G>A CA389592622 NM_001308133.2:c.1440G>C CA389592623 NM_001308133.2:c.1440G>T