Canonical Allele Identifier: PA2826330553
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 182469
ClinVar RCV Id: RCV000160470 RCV001167422 RCV000205386 RCV002326920
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Pro147Leu
CA299136
NM_001243743.2:c.440C>T