Canonical Allele Identifier: PA159389
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 134296
ClinVar RCV Id: RCV000120969 RCV000224016 RCV000566496 RCV000709083 RCV000988205 RCV001082314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ser386Pro
CA159387
NM_000136.3:c.1156T>C