Canonical Allele Identifier: PA2580109753
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784760
ClinVar RCV Id: RCV002419789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000391.1:p.Met677Thr
CA406362791
NM_000400.4:c.2030T>C