Canonical Allele Identifier: PA2826924957
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1510752
ClinVar RCV Id: RCV002014099

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Leu500Gln
CA389592749
NM_001308133.2:c.1499T>A