Canonical Allele Identifier: PA2825055646
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 3230394
ClinVar RCV Id: RCV004520545

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Met254Lys
CA374109345
NM_000136.3:c.761T>A