Canonical Allele Identifier: PA1139754365
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 946206
ClinVar RCV Id: RCV001217021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Glu153Lys
CA380059015
NM_022725.4:c.457G>A