Canonical Allele Identifier: PA2826658052
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 95287
ClinVar RCV Id: RCV000081301 RCV001187167 RCV001212011 RCV002390237 RCV003997207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Gly393_Asp394insGlu
CA017229
NM_001282624.2:c.1179_1181dup