Canonical Allele Identifier: PA2826330557
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 423119
ClinVar RCV Id: RCV000477975
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Gly148Ala
CA16618889
NM_001243743.2:c.443G>C