Canonical Allele Identifier: PA158769
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134100

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000391.1:p.Ala635Val
CA158767
NM_000400.4:c.1904C>T