Canonical Allele Identifier: PA658807123
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 539301
ClinVar RCV Id: RCV000649010 RCV002256452 RCV002269298 RCV003937954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Gln95Arg
CA3771372
NM_021922.3:c.284A>G