Canonical Allele Identifier: PA916015191
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456125
ClinVar RCV Id: RCV000545703 RCV000765321 RCV002476091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg1321His
CA8250848
NM_001286167.3:c.3962G>A