Canonical Allele Identifier: PA2825056265
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1389407
ClinVar RCV Id: RCV001917359 RCV002397850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Lys552Gln
CA374104264
NM_000136.3:c.1654A>C