Canonical Allele Identifier: PA2826658286
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 245817
ClinVar RCV Id: RCV000236179 RCV001079756 RCV001182288 RCV002392726 RCV003998902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg25Leu
CA054268
NM_001282625.2:c.74G>T