Canonical Allele Identifier: PA916014999
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134260
ClinVar RCV Id: RCV000120933 RCV000668462 RCV002514634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg894Lys
CA159290
NM_001286167.3:c.2681G>A