Canonical Allele Identifier: PA645402588
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 418188
ClinVar RCV Id: RCV000484866 RCV000988211 RCV001017686 RCV001243848 RCV003409651
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ser280Leu
CA5137627
NM_000136.3:c.839C>T