Canonical Allele Identifier: PA299171
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182480
ClinVar RCV Id: RCV000160481 RCV000571755 RCV000709088 RCV001194155 RCV001085038 RCV001355168 RCV003492652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Glu273Lys
CA299169
NM_000136.3:c.817G>A