Canonical Allele Identifier: PA2573278436
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1433588
ClinVar RCV Id: RCV001946093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Lys218Glu
CA16622023
NM_021922.3:c.652A>G