Canonical Allele Identifier: PA097893
Gene: ERCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 68752
ClinVar RCV Id: RCV000024268 RCV000059645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000073.1:p.Trp361Cys
CA129810
NM_000082.4:c.1083G>T
CA359822538
NM_000082.4:c.1083G>C