Canonical Allele Identifier: PA645431374
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313204
ClinVar RCV Id: RCV000280719 RCV001030476 RCV001597071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.His747Arg
CA7169295
NM_020937.4:c.2240A>G