Canonical Allele Identifier: PA916015096
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134266
ClinVar RCV Id: RCV000120939 RCV000667894 RCV002514635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ala1141Asp
CA159307
NM_001286167.3:c.3422C>A