Canonical Allele Identifier: PA336596
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 216290
ClinVar RCV Id: RCV000196637 RCV000709089 RCV001025536 RCV001818486 RCV002478703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Val223Ala
CA336594
NM_000136.3:c.668T>C