Canonical Allele Identifier: PA159416
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 134306
ClinVar RCV Id: RCV000120980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg209Leu
CA159414
NM_000136.3:c.626G>T