Canonical Allele Identifier: PA2825744001
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1763459
ClinVar RCV Id: RCV002447554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124339.1:p.Arg258Leu
CA406373737
NM_001130867.2:c.773G>T