Canonical Allele Identifier: PA2825054587
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1710959
ClinVar RCV Id: RCV002292246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Glu1178Lys
CA397485759
NM_000135.4:c.3532G>A