Canonical Allele Identifier: PA2580431292
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1980049
ClinVar RCV Id: RCV002780151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Glu207Lys
CA363773302
NM_021922.3:c.619G>A