Canonical Allele Identifier: PA159262
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134249
ClinVar RCV Id: RCV000120922 RCV000667865 RCV001243928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Arg670Cys
CA159260
NM_000135.4:c.2008C>T