Canonical Allele Identifier: PA2826331196
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127548
ClinVar RCV Id: RCV000196771 RCV000572525 RCV000988209 RCV001195051 RCV001818268 RCV000709085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Ile312Val
CA287233
NM_001243743.2:c.934A>G