Allele Registry

Canonical Allele Identifier: PA916052586

Gene: FANCM HGNC NCBI

ClinVar Variation Id: 643944

HGVS (amino-acid)	Matching Registered Transcripts
NP_065988.1:p.Met506Ile	CA389592621 NM_020937.4:c.1518G>A CA389592622 NM_020937.4:c.1518G>C CA389592623 NM_020937.4:c.1518G>T