Canonical Allele Identifier: PA915955226
Gene: ERCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007235.1:p.Ala160Val
CA219852
NM_001007234.3:c.479C>T