Canonical Allele Identifier: PA2826926826
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 3092830
ClinVar RCV Id: RCV004383747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.Thr517Lys
CA7169079
NM_001308134.2:c.1550C>A