Canonical Allele Identifier: PA645403680
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408185
ClinVar RCV Id: RCV000466659 RCV000503748 RCV001172102 RCV001118714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Thr126Arg
CA8253047
NM_000135.4:c.377C>G