Canonical Allele Identifier: PA2825329332
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456139
ClinVar RCV Id: RCV000532298 RCV000764090 RCV001797096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018122.1:p.His292Asp
CA8252711
NM_001018112.2:c.874C>G