Canonical Allele Identifier: PA658660508
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 456161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Leu110Pro
CA5137779
NM_000136.3:c.329T>C