Canonical Allele Identifier: PA2828688441
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 408254
ClinVar RCV Id: RCV000470517 RCV001115869 RCV003151064
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363840.1:p.Gly53Ala
CA7722518
NM_001376911.1:c.158G>C