Canonical Allele Identifier: PA2580439391
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 2081761
ClinVar RCV Id: RCV002995596
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Ala1523Glu
CA259634556
NM_020937.4:c.4568C>A