Canonical Allele Identifier: PA2580456739
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 2131272
ClinVar RCV Id: RCV003048125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Asn154Lys
CA380059001
NM_022725.4:c.462C>G
CA380059002
NM_022725.4:c.462C>A