Canonical Allele Identifier: PA916015138
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 216278
ClinVar RCV Id: RCV000198937 RCV000765322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gln1235Glu
CA338301
NM_001286167.3:c.3703C>G