Canonical Allele Identifier: PA2826925865
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 2038723
ClinVar RCV Id: RCV002907696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Glu1495Val
CA389608170
NM_001308133.2:c.4484A>T