Canonical Allele Identifier: PA916015031
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 224986
ClinVar RCV Id: RCV000210699 RCV000458460 RCV000675145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Cys981Arg
CA358217
NM_001286167.3:c.2941T>C