Canonical Allele Identifier: PA159413
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127544
ClinVar RCV Id: RCV000120979 RCV000200372 RCV000570280 RCV000709090 RCV000988214 RCV001195037 RCV001356599 RCV003945045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Pro211Arg
CA159411
NM_000136.3:c.632C>G