Canonical Allele Identifier: PA645402820
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 234672
ClinVar RCV Id: RCV000214884 RCV001012385 RCV000543270 RCV001355318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Lys545Arg
CA5137290
NM_000136.3:c.1634A>G