Canonical Allele Identifier: PA645467639
Gene: ERCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 354022
ClinVar RCV Id: RCV000394430 RCV000967836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000073.1:p.Asp50Gly
CA3277948
NM_000082.4:c.149A>G