Canonical Allele Identifier: PA299205
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182492
ClinVar RCV Id: RCV000160494 RCV000630940 RCV001012509 RCV003153437 RCV001818357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg548Gln
CA299203
NM_000136.3:c.1643G>A