Canonical Allele Identifier: PA658660478
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 456150
ClinVar RCV Id: RCV000527400 RCV002323915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Val38Leu
CA374340307
NM_000136.3:c.112G>T
CA374340308
NM_000136.3:c.112G>C