Canonical Allele Identifier: PA097846
Gene: ERCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717
ClinVar RCV Id: RCV000001787 RCV000059647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000073.1:p.Ala160Val
CA219852
NM_000082.4:c.479C>T