Canonical Allele Identifier: PA100854
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 55829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Arg589Trp
CA143941
NM_005236.3:c.1765C>T