Canonical Allele Identifier: PA2826658647
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66901
ClinVar RCV Id: RCV000057411 RCV000503619 RCV000556738 RCV000620401 RCV003993783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg166Pro
CA018166
NM_001282625.2:c.497G>C