Canonical Allele Identifier: PA2826329819
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 234311
ClinVar RCV Id: RCV000221946 RCV000477104 RCV000575115 RCV001358152 RCV003144167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ala158Pro
CA10577378
NM_001243743.2:c.472G>C