Canonical Allele Identifier: PA2573280611
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1447638
ClinVar RCV Id: RCV001979922 RCV004529063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Gln602Arg
CA389594806
NM_020937.4:c.1805A>G