Canonical Allele Identifier: PA916006616
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 651971
ClinVar RCV Id: RCV000807428
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Gly524Ser
CA5137295
NM_001243743.2:c.1570G>A