Canonical Allele Identifier: PA2826924845
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1979542
ClinVar RCV Id: RCV002766394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Arg379Gln
CA7168971
NM_001308133.2:c.1136G>A