Canonical Allele Identifier: PA2573280985
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1691901
ClinVar RCV Id: RCV002259175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Glu1533Lys
CA259634575
NM_020937.4:c.4597G>A