Canonical Allele Identifier: PA2825055013
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 656395
ClinVar RCV Id: RCV000812802
ClinVar Variation Id: 803291
ClinVar RCV Id: RCV000989669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Gln1389His
CA397484248
NM_000135.4:c.4167G>T
CA397484249
NM_000135.4:c.4167G>C