Canonical Allele Identifier: PA916063650
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 414868
ClinVar RCV Id: RCV000466767 RCV001119038 RCV003401499 RCV003902684
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Gly655Arg
CA7723227
NM_018193.3:c.1963G>A
CA393748775
NM_018193.3:c.1963G>C