Canonical Allele Identifier: PA645402780
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 367609
ClinVar RCV Id: RCV000284344 RCV000519902 RCV001012118 RCV001095337 RCV001821124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Thr515Ser
CA5137299
NM_000136.3:c.1544C>G
CA374104833
NM_000136.3:c.1543A>T