Canonical Allele Identifier: PA2826658487
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 408995
ClinVar RCV Id: RCV000472865 RCV000598315 RCV001524820 RCV002436430 RCV002489054 RCV003387849 RCV004000799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Lys97Thr
CA16609882
NM_001282625.2:c.290A>C