Canonical Allele Identifier: PA158914
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 134150
ClinVar RCV Id: RCV000120823 RCV000459235 RCV001034544 RCV001117661 RCV002258800 RCV002515862
ClinVar Variation Id: 885831
ClinVar RCV Id: RCV001117660 RCV002497527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Gln496His
CA158912
NM_005236.3:c.1488A>T
CA7910476
NM_005236.3:c.1488A>C