Canonical Allele Identifier: PA2826710804
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 552870
ClinVar RCV Id: RCV000668215 RCV001246549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gly115Arg
CA8253058
NM_001286167.3:c.343G>A
CA397481011
NM_001286167.3:c.343G>C