Canonical Allele Identifier: PA2580431298
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 2072640
ClinVar RCV Id: RCV002967252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Arg233Lys
CA363773626
NM_021922.3:c.698G>A