Canonical Allele Identifier: PA916035487
Gene: LIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 211374

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