Canonical Allele Identifier: PA645431492
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313225
ClinVar RCV Id: RCV000367982 RCV000658691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.His1703Arg
CA7169910
NM_020937.4:c.5108A>G