Canonical Allele Identifier: PA2826330010
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 422569
ClinVar RCV Id: RCV000481288
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230672.1:p.Val6Leu
CA16618897
NM_001243743.2:c.16G>C
CA374340519
NM_001243743.2:c.16G>T