Canonical Allele Identifier: PA2573162523
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1498705
ClinVar RCV Id: RCV001999351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Ile1396Val
CA397483708
NM_000135.4:c.4186A>G