Canonical Allele Identifier: PA916014939
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134251
ClinVar RCV Id: RCV000120924 RCV000233082 RCV001333235 RCV002225374 RCV003952596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Lys701Glu
CA159266
NM_001286167.3:c.2101A>G