Canonical Allele Identifier: PA2826924660
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313193
ClinVar RCV Id: RCV000338024 RCV000503452 RCV001293001 RCV001706479 RCV004537775
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Thr176Ile
CA7168797
NM_001308133.2:c.527C>T