Canonical Allele Identifier: PA916014987
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 425115
ClinVar RCV Id: RCV000487984 RCV001865499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg880Gly
CA16621696
NM_001286167.3:c.2638C>G