Canonical Allele Identifier: PA2573283386
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1386452
ClinVar RCV Id: RCV001881470
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_073562.1:p.Thr264Ser
CA380058319
NM_022725.4:c.791C>G
CA380058321
NM_022725.4:c.790A>T