Canonical Allele Identifier: PA2825743981
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1762307
ClinVar RCV Id: RCV002427803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124339.1:p.Ile249Phe
CA406373880
NM_001130867.2:c.745A>T