Canonical Allele Identifier: PA2573191079
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1562518
ClinVar RCV Id: RCV002204843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Thr1396Ile
CA8250695
NM_001286167.3:c.4187C>T