Canonical Allele Identifier: PA2826926077
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 241324
ClinVar RCV Id: RCV000253417 RCV000231642 RCV001331161 RCV000658692 RCV002257595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Ile1716Val
CA7169934
NM_001308133.2:c.5146A>G