Canonical Allele Identifier: PA2825055025
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1319517
ClinVar RCV Id: RCV003237517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Lys1398Glu
CA397483653
NM_000135.4:c.4192A>G