Canonical Allele Identifier: PA104325
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 16781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000391.1:p.Ala725Pro
CA126881
NM_000400.4:c.2173G>C