Canonical Allele Identifier: PA158796
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000391.1:p.Thr325Met
CA158794
NM_000400.4:c.974C>T