Canonical Allele Identifier: PA100952
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 929560
ClinVar RCV Id: RCV001194783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Ser786Phe
CA394823163
NM_005236.3:c.2357C>T