Canonical Allele Identifier: PA2826714541
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1159424
ClinVar RCV Id: RCV001503133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg1394Gly
CA8250699
NM_001286167.3:c.4180C>G