Canonical Allele Identifier: PA2825329291
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134294
ClinVar RCV Id: RCV000120967 RCV000308742 RCV001094264 RCV001269374 RCV001705891 RCV002415609
ClinVar Variation Id: 1149717
ClinVar RCV Id: RCV001490045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018122.1:p.Thr266Ala
CA159381
NM_001018112.2:c.796A>G
CA2499223867
NM_001018112.2:c.795_796delinsTG