Canonical Allele Identifier: PA2826780905
Gene: ERCC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 68752
ClinVar RCV Id: RCV000024268 RCV000059645
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001277214.1:p.Trp208Cys
CA129810
NM_001290285.1:c.624G>T
CA359822538
NM_001290285.1:c.624G>C