Canonical Allele Identifier: PA916015020
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408196
ClinVar RCV Id: RCV000466964 RCV000669024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg951Trp
CA8251482
NM_001286167.3:c.2851C>T