Canonical Allele Identifier: PA158932
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 134156
ClinVar RCV Id: RCV000120829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Gly508Glu
CA158930
NM_005236.3:c.1523G>A