Canonical Allele Identifier: PA2825744020
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1764575
ClinVar RCV Id: RCV002373592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124339.1:p.Leu268Pro
CA406373596
NM_001130867.2:c.803T>C