Canonical Allele Identifier: PA158872
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 134136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Ala826Val
CA158870
NM_005236.3:c.2477C>T