Canonical Allele Identifier: PA256209
Gene: FANCC HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Leu496Arg
CA256207
NM_000136.3:c.1487T>G