Canonical Allele Identifier: PA2826658648
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 163866
ClinVar RCV Id: RCV000150939 RCV000653861 RCV000732765 RCV000771896 RCV002336298 RCV002505147 RCV003998206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg166Gln
CA018161
NM_001282625.2:c.497G>A