Allele Registry

Canonical Allele Identifier: PA2826780888

Gene: ERCC8 HGNC NCBI

ClinVar RCV:

RCV000171383

ClinVar Variation:

191197

HGVS (amino-acid)	Matching Registered Transcripts
NP_001277214.1:p.Cys186Tyr	CA236232 NM_001290285.1:c.557G>A