Canonical Allele Identifier: PA284831
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 12043
ClinVar RCV Id: RCV000012823 RCV000058925 RCV001221431 RCV002399319 RCV003421917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Leu554Pro
CA284829
NM_000136.3:c.1661T>C