Canonical Allele Identifier: PA2826924945
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 2130521
ClinVar RCV Id: RCV003044583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Gly488Arg
CA7169072
NM_001308133.2:c.1462G>A
CA389592668
NM_001308133.2:c.1462G>C