Canonical Allele Identifier: PA2499288442
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 1005434
ClinVar RCV Id: RCV001302300 RCV002255642 RCV003238340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Arg221Trp
CA3771461
NM_021922.3:c.661C>T