Canonical Allele Identifier: PA658660537
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 456163
ClinVar RCV Id: RCV000550475 RCV001821481 RCV000566915 RCV001276460 RCV002254930
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Tyr146del
CA5137747
NM_000136.3:c.436_438del