Canonical Allele Identifier: PA2826925476
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 414849
ClinVar RCV Id: RCV000475344 RCV000989208 RCV001569551 RCV001821346 RCV002257746 RCV004535465 RCV003316605 RCV003447530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Arg1073His
CA7169492
NM_001308133.2:c.3218G>A