Canonical Allele Identifier: PA2826924956
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1386332
ClinVar RCV Id: RCV001875276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Leu500Pro
CA7169087
NM_001308133.2:c.1499T>C