Canonical Allele Identifier: PA645401900
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 374688
ClinVar RCV Id: RCV000416265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Met497Val
CA16043849
NM_005236.3:c.1489A>G