Canonical Allele Identifier: PA2826925923
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313221
ClinVar RCV Id: RCV000402989 RCV001030549 RCV002256202 RCV003229827 RCV004544559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Arg1544His
CA7169843
NM_001308133.2:c.4631G>A