Canonical Allele Identifier: PA658660791
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 485542
ClinVar RCV Id: RCV000565785 RCV001853768 RCV001273983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Tyr430del
CA589580888
NM_000136.3:c.1288_1290del