Canonical Allele Identifier: PA2826926791
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1484109
ClinVar RCV Id: RCV002005553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.Met480Lys
CA389592446
NM_001308134.2:c.1439T>A