Canonical Allele Identifier: PA916014902
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408177
ClinVar RCV Id: RCV000476740 RCV000765329 RCV003418177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg591Gln
CA8252114
NM_001286167.3:c.1772G>A