Canonical Allele Identifier: PA159298
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134262
ClinVar RCV Id: RCV000120935 RCV000667206 RCV000872247
ClinVar Variation Id: 376974
ClinVar RCV Id: RCV000431238 RCV001080884 RCV001120358 RCV001821151 RCV003902464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Asp953Glu
CA159296
NM_000135.4:c.2859C>A
CA8251450
NM_000135.4:c.2859C>G