Canonical Allele Identifier: PA2573190742
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1489484
ClinVar RCV Id: RCV001978317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Thr266Glu
CA2573152802
NM_001286167.3:c.796_797delinsGA