Canonical Allele Identifier: PA2573278442
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1691919
ClinVar RCV Id: RCV002255796 RCV002481062 RCV003094195 RCV003896090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Arg219Lys
CA363773464
NM_021922.3:c.656G>A