Canonical Allele Identifier: PA2573278438
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1367807
ClinVar RCV Id: RCV001947485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Lys218Arg
CA3771458
NM_021922.3:c.653A>G