Canonical Allele Identifier: PA2580431293
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 2444831
ClinVar RCV Id: RCV003154175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Gly213Arg
CA363773385
NM_021922.3:c.637G>A
CA363773387
NM_021922.3:c.637G>C