Canonical Allele Identifier: PA339143
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 216287
ClinVar RCV Id: RCV000200177 RCV000218236 RCV000709098 RCV001016913 RCV001818485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Cys10Gly
CA339141
NM_000136.3:c.28T>G