Canonical Allele Identifier: PA2826924980
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 456254
ClinVar RCV Id: RCV000536634 RCV001293939 RCV001584242 RCV001800738 RCV002255431 RCV003492091
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Asp530Gly
CA7169123
NM_001308133.2:c.1589A>G