Canonical Allele Identifier: PA2826925249
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 241318
ClinVar RCV Id: RCV000227957 RCV001536588 RCV002256168 RCV004541448
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Ile813Met
CA7169365
NM_001308133.2:c.2439T>G