Canonical Allele Identifier: PA2827660313
Gene: LIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423109
ClinVar RCV Id: RCV001926487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339528.1:p.Leu644Phe
CA388615253
NM_001352599.2:c.1932A>T
CA388615255
NM_001352599.2:c.1932A>C