Canonical Allele Identifier: PA916015019
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 526433
ClinVar RCV Id: RCV000630961 RCV000666705 RCV001569733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg951Gln
CA8251481
NM_001286167.3:c.2852G>A