Canonical Allele Identifier: PA104429
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1499293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000391.1:p.Arg658His
CA9512956
NM_000400.4:c.1973G>A