Canonical Allele Identifier: PA2826926833
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_001295063.1:p.Leu526Pro
CA7169087
NM_001308134.2:c.1577T>C