Canonical Allele Identifier: PA645403981
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 237058
ClinVar RCV Id: RCV000231055 RCV001274646 RCV002261014 RCV004020741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ser290Tyr
CA8252715
NM_000135.4:c.869C>A