Canonical Allele Identifier: PA645438758
Gene: FANCG HGNC NCBI

Linked Data

ClinVar Variation Id: 239969
ClinVar RCV Id: RCV000228244 RCV000502617 RCV000764833 RCV003955346
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004620.1:p.Gly294Glu
CA5039921
NM_004629.2:c.881G>A