Canonical Allele Identifier: PA916015113
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134271
ClinVar RCV Id: RCV000120944 RCV000862979 RCV001274558 RCV003477508 RCV003975073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg1195Gln
CA159319
NM_001286167.3:c.3584G>A