Canonical Allele Identifier: PA2826924946
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1312560
ClinVar RCV Id: RCV001761448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Ser490Arg
CA389592681
NM_001308133.2:c.1468A>C
CA389592686
NM_001308133.2:c.1470C>A
CA389592687
NM_001308133.2:c.1470C>G