Canonical Allele Identifier: PA158917
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 134151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Ile553Val
CA158915
NM_005236.3:c.1657A>G