Canonical Allele Identifier: PA100863
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 55824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Arg689Ser
CA143933
NM_005236.3:c.2065C>A