Canonical Allele Identifier: PA645402492
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 418577
ClinVar RCV Id: RCV000485063 RCV001066884 RCV002341128
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Ala158Val
CA5137724
NM_000136.3:c.473C>T