Canonical Allele Identifier: PA916006978
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 237076
ClinVar RCV Id: RCV000231342 RCV001026618 RCV001274479 RCV001354988 RCV001551720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Met254Val
CA5137637
NM_001243744.2:c.760A>G