Canonical Allele Identifier: PA158899
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 134145
ClinVar RCV Id: RCV000120818 RCV000728799 RCV001209805 RCV001543122
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Tyr71His
CA158897
NM_005236.3:c.211T>C