Canonical Allele Identifier: PA159530
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 134333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Ser204Leu
CA159528
NM_021922.3:c.611C>T