Allele Registry

Canonical Allele Identifier: PA2825160226

Gene: ERCC2 HGNC NCBI

ClinVar RCV:

RCV004518387

ClinVar Variation:

3231671

HGVS (amino-acid)	Matching Registered Transcripts
NP_000391.1:p.Phe679Leu	CA406362726 NM_000400.4:c.2037T>G CA406362741 NM_000400.4:c.2037T>A CA406362751 NM_000400.4:c.2035T>C