Canonical Allele Identifier: PA2826331729
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 485542
ClinVar RCV Id: RCV000565785 RCV001853768 RCV001273983
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Tyr430del
CA349399
NM_001243743.2:c.1290C>A
CA374107297
NM_001243743.2:c.1290C>G
CA374107304
NM_001243743.2:c.1287C>G
CA374107305
NM_001243743.2:c.1287C>A
CA589580888
NM_001243743.2:c.1288_1290del