Canonical Allele Identifier: PA118989
Gene: LIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002303.2:p.Thr9Ile
CA118987
NM_002312.3:c.26C>T