Canonical Allele Identifier: PA2826714538
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 997461
ClinVar RCV Id: RCV001292617 RCV001859237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg1394His
CA8250696
NM_001286167.3:c.4181G>A