Canonical Allele Identifier: PA2573278446
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1485065
ClinVar RCV Id: RCV002008376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Glu226Ala
CA363773561
NM_021922.3:c.677A>C