Canonical Allele Identifier: PA2825286034
Gene: ERCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 68752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007234.1:p.Trp303Cys
CA129810
NM_001007233.3:c.909G>T
CA359822538
NM_001007233.3:c.909G>C