Canonical Allele Identifier: PA2825051721
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1358367
ClinVar RCV Id: RCV001878607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Gln123Glu
CA397480964
NM_000135.4:c.367C>G