Canonical Allele Identifier: PA2826926351
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 456276
ClinVar RCV Id: RCV000554625 RCV000989207 RCV000763926 RCV001821483 RCV001770408 RCV003338648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.Arg18Gln
CA7168688
NM_001308134.2:c.53G>A