Canonical Allele Identifier: PA916015044
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134263
ClinVar RCV Id: RCV000120936 RCV000862981 RCV001276514 RCV003477505 RCV003975072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gln993Lys
CA159299
NM_001286167.3:c.2977C>A