Canonical Allele Identifier: PA2573169259
Gene: ERCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1497472
ClinVar RCV Id: RCV002019441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000391.1:p.Leu708Val
CA406362173
NM_000400.4:c.2122C>G