Canonical Allele Identifier: PA645429058
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 408153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Ala104Gly
CA3771379
NM_021922.3:c.311C>G