Canonical Allele Identifier: PA658807151
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 517206
ClinVar RCV Id: RCV000609034 RCV000649001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Leu444Pro
CA3771681
NM_021922.3:c.1331T>C