Canonical Allele Identifier: PA2825055327
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730284
ClinVar RCV Id: RCV002326460
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Asn111Ser
CA5137778
NM_000136.3:c.332A>G