Canonical Allele Identifier: PA2573095353
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1319636
ClinVar RCV Id: RCV001885116 RCV003237629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Asn156Asp
CA5924324
NM_022725.4:c.466A>G