Canonical Allele Identifier: PA2826924947
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 840552
ClinVar RCV Id: RCV001042572 RCV001555787 RCV002497374
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Thr491Met
CA7169078
NM_001308133.2:c.1472C>T