Canonical Allele Identifier: PA2825055012
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1524572
ClinVar RCV Id: RCV002031818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Lys1387Glu
CA397484269
NM_000135.4:c.4159A>G