Canonical Allele Identifier: PA158887
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 134141
ClinVar RCV Id: RCV000120814 RCV000474309 RCV001356061 RCV003315750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Gly912Arg
CA158885
NM_005236.3:c.2734G>A
CA394825268
NM_005236.3:c.2734G>C