Canonical Allele Identifier: PA100880
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 55827
ClinVar RCV Id: RCV000049248 RCV001568088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Cys236Arg
CA143938
NM_005236.3:c.706T>C