Canonical Allele Identifier: PA916006923
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 134305
ClinVar RCV Id: RCV000120978 RCV000124962 RCV000179716 RCV000667368 RCV000988215 RCV001356570 RCV001083500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Asp195Val
CA247025
NM_001243744.2:c.584A>T