Canonical Allele Identifier: PA2741839415
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 2585981
ClinVar RCV Id: RCV003368122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230673.1:p.Val117Leu
CA374338914
NM_001243744.2:c.349G>T
CA374338915
NM_001243744.2:c.349G>C