Canonical Allele Identifier: PA658661855
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 456283
ClinVar RCV Id: RCV000547221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Glu183Lys
CA5924312
NM_022725.4:c.547G>A