Canonical Allele Identifier: PA2580105575
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2012164
ClinVar RCV Id: RCV002838954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ile1396Thr
CA397483700
NM_000135.4:c.4187T>C