Canonical Allele Identifier: PA658661900
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 471930
ClinVar RCV Id: RCV000538869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Gly198Arg
CA3771444
NM_021922.3:c.592G>A
CA363773235
NM_021922.3:c.592G>C