Canonical Allele Identifier: PA158938
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 134158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Arg576Thr
CA158936
NM_005236.3:c.1727G>C