Allele Registry

Canonical Allele Identifier: PA2825286018

Gene: ERCC8 HGNC NCBI

ClinVar RCV:

RCV000171383

ClinVar Variation:

191197

HGVS (amino-acid)	Matching Registered Transcripts
NP_001007234.1:p.Cys281Tyr	CA236232 NM_001007233.3:c.842G>A