Allele Registry

Canonical Allele Identifier: PA158935

Gene: ERCC4 HGNC NCBI

ClinVar RCV:

RCV000120830

RCV000989533

RCV001854624

ClinVar Variation:

134157

HGVS (amino-acid)	Matching Registered Transcripts
NP_005227.1:p.Val536Leu	CA158933 NM_005236.3:c.1606G>C CA394811877 NM_005236.3:c.1606G>T