Allele Registry

Canonical Allele Identifier: PA3057553637

Gene: ERCC2 HGNC NCBI

ClinVar RCV:

RCV004982079

ClinVar Variation:

3509861

HGVS (amino-acid)	Matching Registered Transcripts
NP_000391.1:p.Met677Leu	CA406362792 NM_000400.4:c.2029A>T CA406362795 NM_000400.4:c.2029A>C