Canonical Allele Identifier: PA2826925200
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 456259
ClinVar RCV Id: RCV000538182 RCV004541644 RCV001088406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Tyr751Cys
CA7169337
NM_001308133.2:c.2252A>G