Canonical Allele Identifier: PA1139702764
Gene: ERCC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 835496
ClinVar RCV Id: RCV001036389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005227.1:p.Asp705Val
CA394821863
NM_005236.3:c.2114A>T