Canonical Allele Identifier: PA2573283353
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1440055
ClinVar RCV Id: RCV001936785 RCV002473331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Tyr151Asn
CA219086642
NM_022725.4:c.451T>A