Canonical Allele Identifier: PA334696
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 188350
ClinVar RCV Id: RCV000168381 RCV000482249 RCV001025063 RCV003144145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Arg209His
CA334694
NM_000136.3:c.626G>A