Canonical Allele Identifier: PA2573069347
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1319517
ClinVar RCV Id: RCV003237517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Lys1399Arg
CA397483653
NM_001286167.3:c.4196A>G