Canonical Allele Identifier: PA916035487
Gene: LIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 211374
ClinVar RCV Id: RCV000193141 RCV001056709 RCV001110887 RCV002517093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339533.1:p.Ser684Arg
CA206421
NM_001352604.2:c.2052C>G
CA388614528
NM_001352604.2:c.2052C>A
CA388614552
NM_001352604.2:c.2050A>C