Canonical Allele Identifier: PA158878
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 134138
ClinVar RCV Id: RCV000120811 RCV000476568 RCV000989535 RCV001034545 RCV002257429 RCV002515859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Ala860Asp
CA158876
NM_005236.3:c.2579C>A