Canonical Allele Identifier: PA2830522648
Gene: LIG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1041714
ClinVar RCV Id: RCV001345559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_996820.1:p.Phe742Leu
CA388613742
NM_206937.2:c.2226T>A
CA388613743
NM_206937.2:c.2226T>G
CA388613748
NM_206937.2:c.2224T>C