Canonical Allele Identifier: PA2825744071
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1364771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124339.1:p.Glu293Asp
CA406373173
NM_001130867.2:c.879G>T
CA406373174
NM_001130867.2:c.879G>C