Canonical Allele Identifier: PA891845108
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 583038
ClinVar RCV Id: RCV000707263 RCV002469272 RCV002493251 RCV004026748
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Met16Val
CA374340456
NM_000136.3:c.46A>G