Canonical Allele Identifier: PA2826925869
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 2081761
ClinVar RCV Id: RCV002995596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Ala1497Glu
CA259634556
NM_001308133.2:c.4490C>A