Canonical Allele Identifier: PA2826330179
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 127537
ClinVar RCV Id: RCV000115347 RCV000224234 RCV000197543 RCV000709095 RCV001354572 RCV000563479 RCV003492472 RCV003935098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Val60Ile
CA287202
NM_001243743.2:c.178G>A