Canonical Allele Identifier: PA159583
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 134354
ClinVar RCV Id: RCV000121028 RCV000232655 RCV000857633 RCV001094015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Asp125Asn
CA159581
NM_022725.4:c.373G>A