Allele Registry

Canonical Allele Identifier: PA916017520

Gene: ERCC8 HGNC NCBI

ClinVar RCV:

RCV000001788

RCV000059650

ClinVar Variation:

1718

HGVS (amino-acid)	Matching Registered Transcripts
NP_001277214.1:p.Ala52Pro	CA219858 NM_001290285.1:c.154G>C