Canonical Allele Identifier: PA2829897906
Gene: FANCI HGNC NCBI

Linked Data

ClinVar Variation Id: 238321
ClinVar RCV Id: RCV000233382 RCV001119128 RCV003967621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060663.2:p.Thr1019Met
CA7723642
NM_018193.3:c.3056C>T