Canonical Allele Identifier: PA645429122
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 414821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Met437Thr
CA3771662
NM_021922.3:c.1310T>C