Canonical Allele Identifier: PA2826925165
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313204
ClinVar RCV Id: RCV000280719 RCV001030476 RCV001597071
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.His721Arg
CA7169295
NM_001308133.2:c.2162A>G