Canonical Allele Identifier: PA915955221
Gene: ERCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 354022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007235.1:p.Asp50Gly
CA3277948
NM_001007234.3:c.149A>G