Canonical Allele Identifier: PA916014772
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321369
ClinVar RCV Id: RCV000280680 RCV000660417 RCV001753780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Leu193Val
CA8252926
NM_001286167.3:c.577C>G