Canonical Allele Identifier: PA2826924954
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1684728
ClinVar RCV Id: RCV002247820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Glu498Gly
CA389592736
NM_001308133.2:c.1493A>G