Canonical Allele Identifier: PA2825329057
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_001018122.1:p.Thr126Arg
CA8253047
NM_001018112.2:c.377C>G