Canonical Allele Identifier: PA2573280578
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_065988.1:p.Glu524Gly
CA389592736
NM_020937.4:c.1571A>G