Canonical Allele Identifier: PA645431497
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 241324
ClinVar RCV Id: RCV000253417 RCV000231642 RCV001331161 RCV000658692 RCV002257595
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Ile1742Val
CA7169934
NM_020937.4:c.5224A>G