Canonical Allele Identifier: PA2580193571
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1962086
ClinVar RCV Id: RCV002725871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Thr1396Ala
CA397483739
NM_001286167.3:c.4186A>G