Canonical Allele Identifier: PA2825286040
Gene: ERCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 354013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007234.1:p.Val311Leu
CA3277626
NM_001007233.3:c.931G>C