Canonical Allele Identifier: PA159386
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 134295
ClinVar RCV Id: RCV000120968 RCV000766565 RCV001009799 RCV001300842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Asp355His
CA159384
NM_000136.3:c.1063G>C