Canonical Allele Identifier: PA2825526107
Gene: LIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1012117
ClinVar RCV Id: RCV001310020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091738.1:p.Pro647Ser
CA256180357
NM_001098268.2:c.1939C>T